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

A Study to Assess the Safety and Effectiveness of SJP-0035 for the Treatment of Patients With Dry Eye Disease
A Double-Masked, Randomized, Multicenter, Placebo-Controlled, Parallel-Group Study to Assess the Safety and Efficacy of SJP-0035 0.001% for the Treatment of Patients With Dry Eye Disease (DELTA-1 Study)
Status: Enrolling
Updated:  12/31/1969
Southern Utah Medical Research, Suite 100, 292 South 1470 East
mi
from
Saint George, UT
A Study to Assess the Safety and Effectiveness of SJP-0035 for the Treatment of Patients With Dry Eye Disease
A Double-Masked, Randomized, Multicenter, Placebo-Controlled, Parallel-Group Study to Assess the Safety and Efficacy of SJP-0035 0.001% for the Treatment of Patients With Dry Eye Disease (DELTA-1 Study)
Status: Enrolling
Updated: 12/31/1969
Southern Utah Medical Research, Suite 100, 292 South 1470 East
mi
from
Saint George, UT
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A Study to Assess the Safety and Effectiveness of SJP-0035 for the Treatment of Patients With Dry Eye Disease
A Double-Masked, Randomized, Multicenter, Placebo-Controlled, Parallel-Group Study to Assess the Safety and Efficacy of SJP-0035 0.001% for the Treatment of Patients With Dry Eye Disease (DELTA-1 Study)
Status: Enrolling
Updated:  12/31/1969
Virginia Eye Consultants, 241 Corporate Boulevard
mi
from
Norfolk, VA
A Study to Assess the Safety and Effectiveness of SJP-0035 for the Treatment of Patients With Dry Eye Disease
A Double-Masked, Randomized, Multicenter, Placebo-Controlled, Parallel-Group Study to Assess the Safety and Efficacy of SJP-0035 0.001% for the Treatment of Patients With Dry Eye Disease (DELTA-1 Study)
Status: Enrolling
Updated: 12/31/1969
Virginia Eye Consultants, 241 Corporate Boulevard
mi
from
Norfolk, VA
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Evaluation of Effect of Doxycycline Verses Placebo on Retinal Function and Diabetic Retinopathy
Proof-of-Concept 2 (POC2): Evaluation of Effect of Doxycycline Verses Placebo on Retinal Function and Diabetic Retinopathy Progression in Patients With Mild to Moderate Non-Proliferative Diabetic Retinopathy
Status: Enrolling
Updated:  12/31/1969
Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
Evaluation of Effect of Doxycycline Verses Placebo on Retinal Function and Diabetic Retinopathy
Proof-of-Concept 2 (POC2): Evaluation of Effect of Doxycycline Verses Placebo on Retinal Function and Diabetic Retinopathy Progression in Patients With Mild to Moderate Non-Proliferative Diabetic Retinopathy
Status: Enrolling
Updated: 12/31/1969
Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
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CAREN Argus Rehab (CARE) Study
Comprehensive Visual and Mobility Training After Retinal Prosthesis Surgery
Status: Enrolling
Updated:  12/31/1969
Cleveland Clinic
mi
from
Cleveland, OH
CAREN Argus Rehab (CARE) Study
Comprehensive Visual and Mobility Training After Retinal Prosthesis Surgery
Status: Enrolling
Updated: 12/31/1969
Cleveland Clinic
mi
from
Cleveland, OH
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Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated:  12/31/1969
Cornea & Cataract Consultants of Arizona
mi
from
Phoenix, AZ
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated: 12/31/1969
Cornea & Cataract Consultants of Arizona
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated:  12/31/1969
Eye Research Foundation
mi
from
Newport Beach, CA
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated: 12/31/1969
Eye Research Foundation
mi
from
Newport Beach, CA
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Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated:  12/31/1969
Eye Care Insititute
mi
from
Louisville, KY
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated: 12/31/1969
Eye Care Insititute
mi
from
Louisville, KY
Click here to add this to my saved trials
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated:  12/31/1969
Central Maine Eye Care
mi
from
Lewiston, ME
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated: 12/31/1969
Central Maine Eye Care
mi
from
Lewiston, ME
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Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated:  12/31/1969
Andover Eye Associates
mi
from
Andover, MA
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated: 12/31/1969
Andover Eye Associates
mi
from
Andover, MA
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Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated:  12/31/1969
Vita Eye Clinic
mi
from
Shelby, NC
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated: 12/31/1969
Vita Eye Clinic
mi
from
Shelby, NC
Click here to add this to my saved trials
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated:  12/31/1969
Total Eye Care, PA
mi
from
Memphis, TN
Study of SkQ1 as Treatment for Dry-eye Syndrome
A Phase 3, Multi-Center, Randomized, Double-Masked, Placebo-Controlled Clinical Study to Assess the Safety and Efficacy of SkQ1 Ophthalmic Solution for the Treatment of Dry Eye Syndrome
Status: Enrolling
Updated: 12/31/1969
Total Eye Care, PA
mi
from
Memphis, TN
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A Prospective Clinical Study Assessing the Effects of Tetracycline Antibiotic on Tear Film and Tear Lipid Composition Within a Population of Patients Diagnosed With Blepharitis and Dry Eye Disease
A Prospective Clinical Study Assessing the Effects of Tetracycline Antibiotic on Tear Film and Tear Lipid Composition Within a Population of Patients Diagnosed With Blepharitis and Dry Eye Disease
Status: Enrolling
Updated:  12/31/1969
UT Southwestern Medical Center
mi
from
Dallas, TX
A Prospective Clinical Study Assessing the Effects of Tetracycline Antibiotic on Tear Film and Tear Lipid Composition Within a Population of Patients Diagnosed With Blepharitis and Dry Eye Disease
A Prospective Clinical Study Assessing the Effects of Tetracycline Antibiotic on Tear Film and Tear Lipid Composition Within a Population of Patients Diagnosed With Blepharitis and Dry Eye Disease
Status: Enrolling
Updated: 12/31/1969
UT Southwestern Medical Center
mi
from
Dallas, TX
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Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections
Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections
Status: Enrolling
Updated:  12/31/1969
The Mayo Clinic
mi
from
Rochester, MN
Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections
Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections
Status: Enrolling
Updated: 12/31/1969
The Mayo Clinic
mi
from
Rochester, MN
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Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Waterbury, CT
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Waterbury, CT
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Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Louisville, KY
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Louisville, KY
Click here to add this to my saved trials
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Augusta, ME
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Augusta, ME
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Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Lewiston, ME
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Lewiston, ME
Click here to add this to my saved trials
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Andover, MA
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Andover, MA
Click here to add this to my saved trials
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Lancaster, MA
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Lancaster, MA
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Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Quincy, MA
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Quincy, MA
Click here to add this to my saved trials
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Wakefield, MA
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Wakefield, MA
Click here to add this to my saved trials
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Winchester, MA
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Winchester, MA
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Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Derry, NH
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Derry, NH
Click here to add this to my saved trials
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Manchester, NH
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Manchester, NH
Click here to add this to my saved trials
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Memphis, TN
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Memphis, TN
Click here to add this to my saved trials
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated:  12/31/1969
OPUS-1 Investigational Site
mi
from
Norfolk, VA
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
A Phase 3, Multicenter, Randomized, Double- Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of SAR 1118 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye (OPUS-1)
Status: Enrolling
Updated: 12/31/1969
OPUS-1 Investigational Site
mi
from
Norfolk, VA
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KETODEX for Emergence Delirium in Children Undergoing Outpatient Strabismus Surgery
KETODEX for Emergence Delirium in Children Undergoing Outpatient Strabismus Surgery
Status: Enrolling
Updated:  12/31/1969
Ochsner Main Campus
mi
from
Jefferson, LA
KETODEX for Emergence Delirium in Children Undergoing Outpatient Strabismus Surgery
KETODEX for Emergence Delirium in Children Undergoing Outpatient Strabismus Surgery
Status: Enrolling
Updated: 12/31/1969
Ochsner Main Campus
mi
from
Jefferson, LA
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MiBo ThermoFlo Lid Temperature Evaluation
MiBo ThermoFlo Lid Temperature Evaluation
Status: Enrolling
Updated:  12/31/1969
University of Houston, College of Optometry
mi
from
Houston, TX
MiBo ThermoFlo Lid Temperature Evaluation
MiBo ThermoFlo Lid Temperature Evaluation
Status: Enrolling
Updated: 12/31/1969
University of Houston, College of Optometry
mi
from
Houston, TX
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Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Longwood, FL
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Longwood, FL
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Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
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Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Johns Creek, GA
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Johns Creek, GA
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DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
San Diego, CA
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
San Diego, CA
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DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Longwood, FL
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Longwood, FL
Click here to add this to my saved trials
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
Click here to add this to my saved trials
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Bloomington, IL
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Bloomington, IL
Click here to add this to my saved trials
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Brentwood, TN
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Brentwood, TN
Click here to add this to my saved trials
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Memphis, TN
DD T2 Daily Disposable Registration Trial
DD T2 Daily Disposable Registration Trial
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Memphis, TN
Click here to add this to my saved trials
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
Click here to add this to my saved trials
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Pensacola, FL
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Pensacola, FL
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Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Johns Creek, GA
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Clinical Comparison of 4 Daily Disposable Soft Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Johns Creek, GA
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Clinical Comparison of Two Daily Disposable Soft Contact Lenses
Clinical Comparison of Two Daily Disposable Soft Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
Clinical Comparison of Two Daily Disposable Soft Contact Lenses
Clinical Comparison of Two Daily Disposable Soft Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
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Clinical Validation of DACP Digital Design
Clinical Validation of DACP Digital Design
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Bloomington, IL
Clinical Validation of DACP Digital Design
Clinical Validation of DACP Digital Design
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Bloomington, IL
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Clinical Validation of DACP Digital Design
Clinical Validation of DACP Digital Design
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Powell, OH
Clinical Validation of DACP Digital Design
Clinical Validation of DACP Digital Design
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Powell, OH
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Clinical Validation of DACP Digital Design
Clinical Validation of DACP Digital Design
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Brentwood, TN
Clinical Validation of DACP Digital Design
Clinical Validation of DACP Digital Design
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Brentwood, TN
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Clinical Validation of DACP Digital Design
Clinical Validation of DACP Digital Design
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Memphis, TN
Clinical Validation of DACP Digital Design
Clinical Validation of DACP Digital Design
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Memphis, TN
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Multifocal Visual Performance Study
Multifocal Visual Performance Study - Seamless Transition With Precision Profile MF Lenses
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Houston, TX
Multifocal Visual Performance Study
Multifocal Visual Performance Study - Seamless Transition With Precision Profile MF Lenses
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Houston, TX
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Multifocal Visual Performance Study
Multifocal Visual Performance Study - Seamless Transition With Precision Profile MF Lenses
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Birmingham,
Multifocal Visual Performance Study
Multifocal Visual Performance Study - Seamless Transition With Precision Profile MF Lenses
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Birmingham,
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Pilot Study of TearCare System - Long-Term Extension
Pilot Study of TearCare System - Long-Term Extension
Status: Enrolling
Updated:  12/31/1969
Central Eye Care, Ltd.
mi
from
Arlington Heights, IL
Pilot Study of TearCare System - Long-Term Extension
Pilot Study of TearCare System - Long-Term Extension
Status: Enrolling
Updated: 12/31/1969
Central Eye Care, Ltd.
mi
from
Arlington Heights, IL
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Performance Assessment of a Modified Daily Disposable Contact Lens
Performance Assessment of a Modified Daily Disposable Contact Lens
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Orlando, FL
Performance Assessment of a Modified Daily Disposable Contact Lens
Performance Assessment of a Modified Daily Disposable Contact Lens
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Orlando, FL
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Performance Assessment of a Modified Daily Disposable Contact Lens
Performance Assessment of a Modified Daily Disposable Contact Lens
Status: Enrolling
Updated:  12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
Performance Assessment of a Modified Daily Disposable Contact Lens
Performance Assessment of a Modified Daily Disposable Contact Lens
Status: Enrolling
Updated: 12/31/1969
Alcon Investigative Site
mi
from
Maitland, FL
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