Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
9,144
archived clinical trials in
Ocular

Validation of TearLab Osmometer - Human Factor Usability Report
Validation of TearLab Osmometer - Human Factor Usability Report
Status: Enrolling
Updated:  3/14/2016
Kentucky Lion Eye Center, University of Louisville
mi
from
Louisville, KY
Validation of TearLab Osmometer - Human Factor Usability Report
Validation of TearLab Osmometer - Human Factor Usability Report
Status: Enrolling
Updated: 3/14/2016
Kentucky Lion Eye Center, University of Louisville
mi
from
Louisville, KY
Click here to add this to my saved trials
Validation of TearLab Osmometer - Human Factor Usability Report
Validation of TearLab Osmometer - Human Factor Usability Report
Status: Enrolling
Updated:  3/14/2016
The Ohio State University College of Optometry
mi
from
Columbus, OH
Validation of TearLab Osmometer - Human Factor Usability Report
Validation of TearLab Osmometer - Human Factor Usability Report
Status: Enrolling
Updated: 3/14/2016
The Ohio State University College of Optometry
mi
from
Columbus, OH
Click here to add this to my saved trials
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated:  3/14/2016
Gordon Binder Weiss Vision Institute
mi
from
San Diego, CA
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated: 3/14/2016
Gordon Binder Weiss Vision Institute
mi
from
San Diego, CA
Click here to add this to my saved trials
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated:  3/14/2016
Kentucky Lion Eye Center
mi
from
Louisville, KY
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated: 3/14/2016
Kentucky Lion Eye Center
mi
from
Louisville, KY
Click here to add this to my saved trials
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated:  3/14/2016
Pepose Vision Institute
mi
from
Chesterfield, MO
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated: 3/14/2016
Pepose Vision Institute
mi
from
Chesterfield, MO
Click here to add this to my saved trials
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated:  3/14/2016
Tauber Eye Clinic
mi
from
Kansas City, MO
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated: 3/14/2016
Tauber Eye Clinic
mi
from
Kansas City, MO
Click here to add this to my saved trials
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated:  3/14/2016
Mundorf Eye Center
mi
from
Charlotte, NC
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated: 3/14/2016
Mundorf Eye Center
mi
from
Charlotte, NC
Click here to add this to my saved trials
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated:  3/14/2016
Ohio State University
mi
from
Columbus, OH
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated: 3/14/2016
Ohio State University
mi
from
Columbus, OH
Click here to add this to my saved trials
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated:  3/14/2016
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
mi
from
Paris,
TearLab Core Validation Study to Establish Referent Values for Dry Eye Disease
A Prospective Study to Establish Normative Values, Demographic Variations, Referent Diagnostic Values and Disease Severity Correlations for Dry Eye Disease and TearLab Osmometry.
Status: Enrolling
Updated: 3/14/2016
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
mi
from
Paris,
Click here to add this to my saved trials
Novel Drug Delivery Technique Via Retroject Device
Novel Drug Delivery Technique for Glaucoma Patients
Status: Enrolling
Updated:  3/15/2016
Duke University Eye Center
mi
from
Durham, NC
Novel Drug Delivery Technique Via Retroject Device
Novel Drug Delivery Technique for Glaucoma Patients
Status: Enrolling
Updated: 3/15/2016
Duke University Eye Center
mi
from
Durham, NC
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Beverly Hills, CA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Beverly Hills, CA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Petaluma, CA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Petaluma, CA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Sacramento, CA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Sacramento, CA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
San Clemente, CA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
San Clemente, CA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Santa Maria, CA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Santa Maria, CA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Parker, CO
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Parker, CO
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Boynton Beach, FL
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Boynton Beach, FL
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Miami, FL
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Miami, FL
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Tampa, FL
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Tampa, FL
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Morrow, GA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Morrow, GA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Indianapolis, IN
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Indianapolis, IN
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Overland Park, KA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Overland Park, KA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Louisville, KY
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Louisville, KY
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Baton Rouge, LA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Baton Rouge, LA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
St. Joseph, MI
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
St. Joseph, MI
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Bloomington, MN
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Bloomington, MN
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Edina, MN
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Edina, MN
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Independence, MO
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Independence, MO
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Kansas City, MO
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Kansas City, MO
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Las Vegas, NV
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Las Vegas, NV
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Winston-Salem, NC
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Winston-Salem, NC
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Cincinnati, OH
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Cincinnati, OH
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Brookville, PA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Brookville, PA
Click here to add this to my saved trials
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Philadelphia, PA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Philadelphia, PA
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Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Pittsburgh, PA
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Pittsburgh, PA
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Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated:  3/16/2016
Clinical Research Facility
mi
from
Beaumont, TX
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent: Extended Follow-up of the Premarket Cohort
Post-approval Study of The Glaukos® iStent® Trabecular Micro-bypass Stent System In Conjunction With Cataract Surgery: Extended Follow-up of the Premarket Cohort
Status: Enrolling
Updated: 3/16/2016
Clinical Research Facility
mi
from
Beaumont, TX
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Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Miami, FL
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Miami, FL
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Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Atlanta, GA
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Atlanta, GA
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Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Chicago, IL
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Chicago, IL
Click here to add this to my saved trials
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Boston, MA
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Boston, MA
Click here to add this to my saved trials
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Cambridge, MA
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Cambridge, MA
Click here to add this to my saved trials
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Omaha, NE
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Omaha, NE
Click here to add this to my saved trials
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
New York, NY
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
New York, NY
Click here to add this to my saved trials
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Winston Salem, NC
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Winston Salem, NC
Click here to add this to my saved trials
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Fargo, ND
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Fargo, ND
Click here to add this to my saved trials
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Cleveland, OH
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Cleveland, OH
Click here to add this to my saved trials
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated:  3/18/2016
Clinical Research Facility
mi
from
Dallas, TX
Suprachoroidal Injection of Triamcinolone Acetonide in Subjects With Macular Edema Following Non-Infectious Uveitis
A Randomized, Masked, Multicenter Study to Assess the Safety and Efficacy of CLS-TA, Triamcinolone Acetonide Injectable Suspension in the Treatment of Subjects With Macular Edema Following Uveitis
Status: Enrolling
Updated: 3/18/2016
Clinical Research Facility
mi
from
Dallas, TX
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Safety and Efficacy Study of Topography-Guided LASIK to Treat Myopia and Hyperopia
Topography-Guided LASIK Using the ALLEGRETTO WAVE Eye-Q 400 Hz Excimer Laser System For the Treatment of Manifest and Cornea Based Myopic and Hyperopic Optical Errors
Status: Enrolling
Updated:  3/18/2016
Milauskas Eye Institute
mi
from
La Quinta, CA
Safety and Efficacy Study of Topography-Guided LASIK to Treat Myopia and Hyperopia
Topography-Guided LASIK Using the ALLEGRETTO WAVE Eye-Q 400 Hz Excimer Laser System For the Treatment of Manifest and Cornea Based Myopic and Hyperopic Optical Errors
Status: Enrolling
Updated: 3/18/2016
Milauskas Eye Institute
mi
from
La Quinta, CA
Click here to add this to my saved trials
Safety and Efficacy Study of Topography-Guided LASIK to Treat Myopia and Hyperopia
Topography-Guided LASIK Using the ALLEGRETTO WAVE Eye-Q 400 Hz Excimer Laser System For the Treatment of Manifest and Cornea Based Myopic and Hyperopic Optical Errors
Status: Enrolling
Updated:  3/18/2016
Gordon -Weiss Vision Institute
mi
from
San Diego, CA
Safety and Efficacy Study of Topography-Guided LASIK to Treat Myopia and Hyperopia
Topography-Guided LASIK Using the ALLEGRETTO WAVE Eye-Q 400 Hz Excimer Laser System For the Treatment of Manifest and Cornea Based Myopic and Hyperopic Optical Errors
Status: Enrolling
Updated: 3/18/2016
Gordon -Weiss Vision Institute
mi
from
San Diego, CA
Click here to add this to my saved trials
Safety and Efficacy Study of Topography-Guided LASIK to Treat Myopia and Hyperopia
Topography-Guided LASIK Using the ALLEGRETTO WAVE Eye-Q 400 Hz Excimer Laser System For the Treatment of Manifest and Cornea Based Myopic and Hyperopic Optical Errors
Status: Enrolling
Updated:  3/18/2016
Woolfson Eye Institute
mi
from
Atlanta, GA
Safety and Efficacy Study of Topography-Guided LASIK to Treat Myopia and Hyperopia
Topography-Guided LASIK Using the ALLEGRETTO WAVE Eye-Q 400 Hz Excimer Laser System For the Treatment of Manifest and Cornea Based Myopic and Hyperopic Optical Errors
Status: Enrolling
Updated: 3/18/2016
Woolfson Eye Institute
mi
from
Atlanta, GA
Click here to add this to my saved trials