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

Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects
Status: Enrolling
Updated:  7/22/2015
Clinical Research Facility
mi
from
San Diego, CA
Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects
Status: Enrolling
Updated: 7/22/2015
Clinical Research Facility
mi
from
San Diego, CA
Click here to add this to my saved trials
Ahmed Versus Baerveldt Comparison Study
Ahmed Versus Baerveldt Comparison Study
Status: Enrolling
Updated:  7/25/2015
University of Miami, Bascom Palmer Eye Institute
mi
from
Miami, FL
Ahmed Versus Baerveldt Comparison Study
Ahmed Versus Baerveldt Comparison Study
Status: Enrolling
Updated: 7/25/2015
University of Miami, Bascom Palmer Eye Institute
mi
from
Miami, FL
Click here to add this to my saved trials
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
Status: Enrolling
Updated:  7/27/2015
Clinical Research Center, University of California, Berkeley
mi
from
Berkeley, CA
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
Status: Enrolling
Updated: 7/27/2015
Clinical Research Center, University of California, Berkeley
mi
from
Berkeley, CA
Click here to add this to my saved trials
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
Status: Enrolling
Updated:  7/27/2015
Center for Contact Lens Research, University of Waterloo
mi
from
Waterloo,
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
Bilateral Dispensing Clinical Trial of Stenfilcon A Against Etafilcon A for Astigmatism
Status: Enrolling
Updated: 7/27/2015
Center for Contact Lens Research, University of Waterloo
mi
from
Waterloo,
Click here to add this to my saved trials
FID# 114657 in Contact Lens Wearers
Evaluation of a Lubricant Eye Drop on Tear Lipid Layer Thickness in Contact Lens Wearers
Status: Enrolling
Updated:  7/28/2015
Contact Alcon Call Center for Trial Locations
mi
from
Fort Worth, TX
FID# 114657 in Contact Lens Wearers
Evaluation of a Lubricant Eye Drop on Tear Lipid Layer Thickness in Contact Lens Wearers
Status: Enrolling
Updated: 7/28/2015
Contact Alcon Call Center for Trial Locations
mi
from
Fort Worth, TX
Click here to add this to my saved trials
Post Approval Study of the AcrySof® IQ Toric Intraocular Lens (IOL) Models SN6AT6-SN6AT9
Post Approval Study of the AcrySof® IQ Toric High Cylinder Power IOL Models SN6AT6-SN6AT9
Status: Enrolling
Updated:  8/3/2015
Contact Alcon Call Center for Trial Locations
mi
from
Fort Worth, TX
Post Approval Study of the AcrySof® IQ Toric Intraocular Lens (IOL) Models SN6AT6-SN6AT9
Post Approval Study of the AcrySof® IQ Toric High Cylinder Power IOL Models SN6AT6-SN6AT9
Status: Enrolling
Updated: 8/3/2015
Contact Alcon Call Center for Trial Locations
mi
from
Fort Worth, TX
Click here to add this to my saved trials
Lubricity Post-Wear - Competitive Lenses Pilot
Lubricity Post-Wear - Pilot Evaluation of Daily Disposable Silicone Hydrogel Contact Lenses After Wear
Status: Enrolling
Updated:  8/3/2015
Contact Alcon Call Center for Trial Locations
mi
from
Fort Worth, TX
Lubricity Post-Wear - Competitive Lenses Pilot
Lubricity Post-Wear - Pilot Evaluation of Daily Disposable Silicone Hydrogel Contact Lenses After Wear
Status: Enrolling
Updated: 8/3/2015
Contact Alcon Call Center for Trial Locations
mi
from
Fort Worth, TX
Click here to add this to my saved trials
Non-invasive Tear Film Dynamic Measurements in Normal, MGD and ADDE Subjects After Saline Instillation
Non-invasive Tear Film Dynamic Measurements in Normal, MGD (Meibomium Gland Dysfunction) and Aqueous Deficient Dry Eye(ADDE) Subjects After Saline Instillation
Status: Enrolling
Updated:  8/5/2015
The Flaum Eye Institute-University of Rochester
mi
from
Rochester, NY
Non-invasive Tear Film Dynamic Measurements in Normal, MGD and ADDE Subjects After Saline Instillation
Non-invasive Tear Film Dynamic Measurements in Normal, MGD (Meibomium Gland Dysfunction) and Aqueous Deficient Dry Eye(ADDE) Subjects After Saline Instillation
Status: Enrolling
Updated: 8/5/2015
The Flaum Eye Institute-University of Rochester
mi
from
Rochester, NY
Click here to add this to my saved trials
A Pilot Study of Functional Optical Coherence Tomography for Ocular Imaging
A Pilot Study of Functional Optical Coherence Tomography for Ocular Imaging
Status: Enrolling
Updated:  8/5/2015
Beckman Laser Institute University of California Irvine
mi
from
Irvine, CA
A Pilot Study of Functional Optical Coherence Tomography for Ocular Imaging
A Pilot Study of Functional Optical Coherence Tomography for Ocular Imaging
Status: Enrolling
Updated: 8/5/2015
Beckman Laser Institute University of California Irvine
mi
from
Irvine, CA
Click here to add this to my saved trials
Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions
Corneal Analysis - Pathology Detection Aid
Status: Enrolling
Updated:  8/13/2015
Shiley Eye Center, University of California, San Diego
mi
from
La Jolla, CA
Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions
Corneal Analysis - Pathology Detection Aid
Status: Enrolling
Updated: 8/13/2015
Shiley Eye Center, University of California, San Diego
mi
from
La Jolla, CA
Click here to add this to my saved trials
Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions
Corneal Analysis - Pathology Detection Aid
Status: Enrolling
Updated:  8/13/2015
Carmel Mountain Vision Care Center
mi
from
San Diego, CA
Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions
Corneal Analysis - Pathology Detection Aid
Status: Enrolling
Updated: 8/13/2015
Carmel Mountain Vision Care Center
mi
from
San Diego, CA
Click here to add this to my saved trials
Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions
Corneal Analysis - Pathology Detection Aid
Status: Enrolling
Updated:  8/13/2015
Dishler Laser Institute
mi
from
Greenwood Village, CO
Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions
Corneal Analysis - Pathology Detection Aid
Status: Enrolling
Updated: 8/13/2015
Dishler Laser Institute
mi
from
Greenwood Village, CO
Click here to add this to my saved trials
Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions
Corneal Analysis - Pathology Detection Aid
Status: Enrolling
Updated:  8/13/2015
Pacific University
mi
from
Forest Grove, OR
Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions
Corneal Analysis - Pathology Detection Aid
Status: Enrolling
Updated: 8/13/2015
Pacific University
mi
from
Forest Grove, OR
Click here to add this to my saved trials
Clinical Study of a UV-Absorbing Acrylic Posterior Chamber Intraocular Lens
A Prospective, Multi-center, Single-phase, Non-randomized, Open-label Study to Assess the Safety and Efficacy of the HMY Model YA-60BB Intraocular Lens (IOL) for the Correction of Aphakia Following Phacoemulsification Cataract Extraction
Status: Enrolling
Updated:  8/17/2015
Contact Hoya Surgical Optics, Inc. for Trial Locations
mi
from
Chino Hills, CA
Clinical Study of a UV-Absorbing Acrylic Posterior Chamber Intraocular Lens
A Prospective, Multi-center, Single-phase, Non-randomized, Open-label Study to Assess the Safety and Efficacy of the HMY Model YA-60BB Intraocular Lens (IOL) for the Correction of Aphakia Following Phacoemulsification Cataract Extraction
Status: Enrolling
Updated: 8/17/2015
Contact Hoya Surgical Optics, Inc. for Trial Locations
mi
from
Chino Hills, CA
Click here to add this to my saved trials
Safety and Tolerability of Artificial Tears in Dry Eye Subjects
Safety and Tolerability of Artificial Tears in Dry Eye Subjects
Status: Enrolling
Updated:  8/17/2015
Clinical Research Facility
mi
from
San Diego, CA
Safety and Tolerability of Artificial Tears in Dry Eye Subjects
Safety and Tolerability of Artificial Tears in Dry Eye Subjects
Status: Enrolling
Updated: 8/17/2015
Clinical Research Facility
mi
from
San Diego, CA
Click here to add this to my saved trials
The Comparison of Cataract Lasers Using the Optimedica Catalys Laser and the Alcon LenSx Laser.
A Prospective Randomized Controlled Clinical Trial Comparing the Intra-operative Effects, Safety, Efficacy and Performance of Two Commercially Available Laser Systems in Patients Undergoing Femtosecond Laser-Assisted Cataract Surgery.
Status: Enrolling
Updated:  8/18/2015
Hoopes Vision
mi
from
Salt Lake City, UT
The Comparison of Cataract Lasers Using the Optimedica Catalys Laser and the Alcon LenSx Laser.
A Prospective Randomized Controlled Clinical Trial Comparing the Intra-operative Effects, Safety, Efficacy and Performance of Two Commercially Available Laser Systems in Patients Undergoing Femtosecond Laser-Assisted Cataract Surgery.
Status: Enrolling
Updated: 8/18/2015
Hoopes Vision
mi
from
Salt Lake City, UT
Click here to add this to my saved trials
Clear Care® Plus vs. PeroxiClear™
Comparison of Two One-Step Hydrogen Peroxide Lens Care Solutions in Symptomatic Contact Lens Wearers
Status: Enrolling
Updated:  8/18/2015
Contact Alcon Call Center for Trial Locations
mi
from
Fort Worth, TX
Clear Care® Plus vs. PeroxiClear™
Comparison of Two One-Step Hydrogen Peroxide Lens Care Solutions in Symptomatic Contact Lens Wearers
Status: Enrolling
Updated: 8/18/2015
Contact Alcon Call Center for Trial Locations
mi
from
Fort Worth, TX
Click here to add this to my saved trials
Adult Providing Access to the Visual Environment (PAVE) - Glaucoma Pilot
Adult Providing Access to the Visual Environment (PAVE) - Glaucoma Pilot
Status: Enrolling
Updated:  8/19/2015
Vanderbilt University
mi
from
Nashville, TN
Adult Providing Access to the Visual Environment (PAVE) - Glaucoma Pilot
Adult Providing Access to the Visual Environment (PAVE) - Glaucoma Pilot
Status: Enrolling
Updated: 8/19/2015
Vanderbilt University
mi
from
Nashville, TN
Click here to add this to my saved trials
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated:  8/20/2015
Family Eye Care Center
mi
from
Campbell, CA
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated: 8/20/2015
Family Eye Care Center
mi
from
Campbell, CA
Click here to add this to my saved trials
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated:  8/20/2015
Golden Optometric Group
mi
from
Whittier, CA
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated: 8/20/2015
Golden Optometric Group
mi
from
Whittier, CA
Click here to add this to my saved trials
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated:  8/20/2015
Drs. Quinn, Foster, &Associates
mi
from
Athens, GA
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated: 8/20/2015
Drs. Quinn, Foster, &Associates
mi
from
Athens, GA
Click here to add this to my saved trials
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated:  8/20/2015
Davis EyeCare Associates
mi
from
Oak Lawn, IL
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated: 8/20/2015
Davis EyeCare Associates
mi
from
Oak Lawn, IL
Click here to add this to my saved trials
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated:  8/20/2015
Kannarr Eye Care LLC
mi
from
Pittsburg, KA
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated: 8/20/2015
Kannarr Eye Care LLC
mi
from
Pittsburg, KA
Click here to add this to my saved trials
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated:  8/20/2015
Complete Eye Care of Medina
mi
from
Medina, MN
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear
Status: Enrolling
Updated: 8/20/2015
Complete Eye Care of Medina
mi
from
Medina, MN
Click here to add this to my saved trials
Combined Cataract Surgery and Planned Descemetorhexis
Combined Cataract Surgery and Planned Descemetorhexis
Status: Enrolling
Updated:  8/20/2015
Medical College of Wisconsin
mi
from
Milwaukee, WI
Combined Cataract Surgery and Planned Descemetorhexis
Combined Cataract Surgery and Planned Descemetorhexis
Status: Enrolling
Updated: 8/20/2015
Medical College of Wisconsin
mi
from
Milwaukee, WI
Click here to add this to my saved trials
A Study Using Intravitreal Injections of a Small Interfering RNA in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated:  8/25/2015
Clinical Research Facility
mi
from
Houston, TX
A Study Using Intravitreal Injections of a Small Interfering RNA in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated: 8/25/2015
Clinical Research Facility
mi
from
Houston, TX
Click here to add this to my saved trials
A Study Using Intravitreal Injections of a Small Interfering RNA in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated:  8/25/2015
mi
from
Sydney,
A Study Using Intravitreal Injections of a Small Interfering RNA in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated: 8/25/2015
mi
from
Sydney,
Click here to add this to my saved trials
Study of Two Formulations of Cyclosporine Ophthalmic Emulsion in Healthy Volunteers and in Patients With Dry Eye
Status: Enrolling
Updated:  8/25/2015
Clinical Research Facility
mi
from
Newport Beach, CA
Study of Two Formulations of Cyclosporine Ophthalmic Emulsion in Healthy Volunteers and in Patients With Dry Eye
Status: Enrolling
Updated: 8/25/2015
Clinical Research Facility
mi
from
Newport Beach, CA
Click here to add this to my saved trials
Workshops for Veterans With Vision and Hearing Loss
Pilot Study: Self Management Groups for Veterans With Dual Sensory Loss
Status: Enrolling
Updated:  8/28/2015
Atlanta VA Medical and Rehab Center, Decatur
mi
from
Decatur, GA
Workshops for Veterans With Vision and Hearing Loss
Pilot Study: Self Management Groups for Veterans With Dual Sensory Loss
Status: Enrolling
Updated: 8/28/2015
Atlanta VA Medical and Rehab Center, Decatur
mi
from
Decatur, GA
Click here to add this to my saved trials
Workshops for Veterans With Vision and Hearing Loss
Pilot Study: Self Management Groups for Veterans With Dual Sensory Loss
Status: Enrolling
Updated:  8/28/2015
VA Portland Health Care System, Portland, OR
mi
from
Portland, OR
Workshops for Veterans With Vision and Hearing Loss
Pilot Study: Self Management Groups for Veterans With Dual Sensory Loss
Status: Enrolling
Updated: 8/28/2015
VA Portland Health Care System, Portland, OR
mi
from
Portland, OR
Click here to add this to my saved trials
Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat Uveitis
Open-Label, Safety and Tolerability Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle in Subjects With Non-Infectious Uveitis
Status: Enrolling
Updated:  8/31/2015
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat Uveitis
Open-Label, Safety and Tolerability Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle in Subjects With Non-Infectious Uveitis
Status: Enrolling
Updated: 8/31/2015
Univ of Nebraska Med Ctr
mi
from
Omaha, NE
Click here to add this to my saved trials
Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat Uveitis
Open-Label, Safety and Tolerability Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle in Subjects With Non-Infectious Uveitis
Status: Enrolling
Updated:  8/31/2015
Cleveland Clinic Foundation
mi
from
Cleveland, OH
Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat Uveitis
Open-Label, Safety and Tolerability Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle in Subjects With Non-Infectious Uveitis
Status: Enrolling
Updated: 8/31/2015
Cleveland Clinic Foundation
mi
from
Cleveland, OH
Click here to add this to my saved trials
Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat Uveitis
Open-Label, Safety and Tolerability Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle in Subjects With Non-Infectious Uveitis
Status: Enrolling
Updated:  8/31/2015
Northwestern University
mi
from
Chicago, IL
Safety Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle to Treat Uveitis
Open-Label, Safety and Tolerability Study of Suprachoroidal Triamcinolone Acetonide Via Microneedle in Subjects With Non-Infectious Uveitis
Status: Enrolling
Updated: 8/31/2015
Northwestern University
mi
from
Chicago, IL
Click here to add this to my saved trials
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated:  8/31/2015
Lexicon Investigational Site
mi
from
Morrow, GA
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated: 8/31/2015
Lexicon Investigational Site
mi
from
Morrow, GA
Click here to add this to my saved trials
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated:  8/31/2015
Lexicon Investigational Site
mi
from
Memphis, TN
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated: 8/31/2015
Lexicon Investigational Site
mi
from
Memphis, TN
Click here to add this to my saved trials
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated:  8/31/2015
Lexicon Investigational Site
mi
from
Austin, TX
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated: 8/31/2015
Lexicon Investigational Site
mi
from
Austin, TX
Click here to add this to my saved trials
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated:  8/31/2015
Lexicon Investigational Site
mi
from
Houston, TX
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated: 8/31/2015
Lexicon Investigational Site
mi
from
Houston, TX
Click here to add this to my saved trials
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated:  8/31/2015
Lexicon Investigational Site
mi
from
San Antonio, TX
Study to Evaluate the Safety, Tolerability, and Efficacy of LX7101 in Subjects With Primary Open-angle Glaucoma or Ocular Hypertension
A Phase 1/2a, Randomized, Parallel-group, Double-masked, Vehicle-controlled, Dose-frequency Escalation Study to Evaluate the Safety, Tolerability, and Intraocular Pressure (IOP)-Lowering Efficacy of Topically Administered LX7101 in Subjects Diagnosed With Primary Open-angle Glaucoma (POAG) or Ocular Hypertension (OHT)
Status: Enrolling
Updated: 8/31/2015
Lexicon Investigational Site
mi
from
San Antonio, TX
Click here to add this to my saved trials
Safety and Effectiveness of Ozurdex Steroid Implants for DME After Vitrectomy Surgery
A Randomized, Pilot Study of the Efficacy and Safety of Ozurdex Steroid Implants in Post-Vitrectomized Eyes in Patients With Diabetic Macular Edema
Status: Enrolling
Updated:  9/1/2015
Lahey Clinic
mi
from
Peabody, MA
Safety and Effectiveness of Ozurdex Steroid Implants for DME After Vitrectomy Surgery
A Randomized, Pilot Study of the Efficacy and Safety of Ozurdex Steroid Implants in Post-Vitrectomized Eyes in Patients With Diabetic Macular Edema
Status: Enrolling
Updated: 9/1/2015
Lahey Clinic
mi
from
Peabody, MA
Click here to add this to my saved trials
A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paediatric Patients With Glaucoma
Status: Enrolling
Updated:  9/2/2015
Clinical Research Facility
mi
from
Louisville, KY
A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paediatric Patients With Glaucoma
Status: Enrolling
Updated: 9/2/2015
Clinical Research Facility
mi
from
Louisville, KY
Click here to add this to my saved trials
A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paediatric Patients With Glaucoma
Status: Enrolling
Updated:  9/2/2015
mi
from
Amiens,
A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paediatric Patients With Glaucoma
Status: Enrolling
Updated: 9/2/2015
mi
from
Amiens,
Click here to add this to my saved trials
Phase 2 Study With Cis-UCA Ophthalmic Solutions in Subjects With Dry Eye
A Phase 2, Multi-Center, Randomized, Double Masked, Placebo Controlled Clinical Study to Assess the Safety and Efficacy of 1.0% and 2.5% Cis-UCA Ophthalmic Solutions in Subjects With Dry Eye
Status: Enrolling
Updated:  9/7/2015
Clinical Research Facility
mi
from
Andover, MA
Phase 2 Study With Cis-UCA Ophthalmic Solutions in Subjects With Dry Eye
A Phase 2, Multi-Center, Randomized, Double Masked, Placebo Controlled Clinical Study to Assess the Safety and Efficacy of 1.0% and 2.5% Cis-UCA Ophthalmic Solutions in Subjects With Dry Eye
Status: Enrolling
Updated: 9/7/2015
Clinical Research Facility
mi
from
Andover, MA
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Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated:  9/10/2015
Byers Eye Institute at Stanford, Stanford Hospital and Clinics
mi
from
Palo Alto, CA
Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated: 9/10/2015
Byers Eye Institute at Stanford, Stanford Hospital and Clinics
mi
from
Palo Alto, CA
Click here to add this to my saved trials
Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated:  9/10/2015
New York Eye & Ear Infirmary
mi
from
New York, NY
Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated: 9/10/2015
New York Eye & Ear Infirmary
mi
from
New York, NY
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Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated:  9/10/2015
Retina Foundation of the Southwest
mi
from
Dallas, TX
Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated: 9/10/2015
Retina Foundation of the Southwest
mi
from
Dallas, TX
Click here to add this to my saved trials
Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated:  9/10/2015
Retina-Vitreaous Associates Medical Group
mi
from
Los Angeles, CA
Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated: 9/10/2015
Retina-Vitreaous Associates Medical Group
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated:  9/10/2015
Retina Research Institute of Texas, LLC
mi
from
Abilene, TX
Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Age-Related Macular Degeneration (AMD)
Phase I/II Study of the Safety and Preliminary Efficacy of Human Central Nervous System Stem Cells (HuCNS-SC) Subretinal Transplantation in Subjects With Geographic Atrophy of Age-Related Macular Degeneration
Status: Enrolling
Updated: 9/10/2015
Retina Research Institute of Texas, LLC
mi
from
Abilene, TX
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Investigation of the Presbia Flexivue Microlens™
Prospective, Non-randomized, Unmasked, Multicenter Clinical Investigation of the Presbia Flexivue Microlens™ for the Improvement of Near Vision in Emmetropic Presbyopes
Status: Enrolling
Updated:  9/10/2015
Assil Eye Institute
mi
from
Beverly Hills, CA
Investigation of the Presbia Flexivue Microlens™
Prospective, Non-randomized, Unmasked, Multicenter Clinical Investigation of the Presbia Flexivue Microlens™ for the Improvement of Near Vision in Emmetropic Presbyopes
Status: Enrolling
Updated: 9/10/2015
Assil Eye Institute
mi
from
Beverly Hills, CA
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Investigation of the Presbia Flexivue Microlens™
Prospective, Non-randomized, Unmasked, Multicenter Clinical Investigation of the Presbia Flexivue Microlens™ for the Improvement of Near Vision in Emmetropic Presbyopes
Status: Enrolling
Updated:  9/10/2015
Gordon-Weiss-Schanzlin
mi
from
La Jolla, CA
Investigation of the Presbia Flexivue Microlens™
Prospective, Non-randomized, Unmasked, Multicenter Clinical Investigation of the Presbia Flexivue Microlens™ for the Improvement of Near Vision in Emmetropic Presbyopes
Status: Enrolling
Updated: 9/10/2015
Gordon-Weiss-Schanzlin
mi
from
La Jolla, CA
Click here to add this to my saved trials
Investigation of the Presbia Flexivue Microlens™
Prospective, Non-randomized, Unmasked, Multicenter Clinical Investigation of the Presbia Flexivue Microlens™ for the Improvement of Near Vision in Emmetropic Presbyopes
Status: Enrolling
Updated:  9/10/2015
Maloney Vision Institute
mi
from
Los Angeles, CA
Investigation of the Presbia Flexivue Microlens™
Prospective, Non-randomized, Unmasked, Multicenter Clinical Investigation of the Presbia Flexivue Microlens™ for the Improvement of Near Vision in Emmetropic Presbyopes
Status: Enrolling
Updated: 9/10/2015
Maloney Vision Institute
mi
from
Los Angeles, CA
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