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

Single-dose Study of ANX007 in Participants With Primary Open-angle Glaucoma
A Phase 1, Open-label, Single-dose, Dose-escalation, Safety, Tolerability, and PK Study of Intravitreal ANX007 in Participants With Primary Open-angle Glaucoma
Status: Enrolling
Updated:  12/31/1969
Byers Eye Institute at Stanford University
mi
from
Palo Alto, CA
Single-dose Study of ANX007 in Participants With Primary Open-angle Glaucoma
A Phase 1, Open-label, Single-dose, Dose-escalation, Safety, Tolerability, and PK Study of Intravitreal ANX007 in Participants With Primary Open-angle Glaucoma
Status: Enrolling
Updated: 12/31/1969
Byers Eye Institute at Stanford University
mi
from
Palo Alto, CA
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ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated:  12/31/1969
Andover Eye Associates
mi
from
Andover, MA
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated: 12/31/1969
Andover Eye Associates
mi
from
Andover, MA
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ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated:  12/31/1969
Cornea Consultants of Arizon
mi
from
Phoenix, AZ
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated: 12/31/1969
Cornea Consultants of Arizon
mi
from
Phoenix, AZ
Click here to add this to my saved trials
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated:  12/31/1969
Eye Site Sacramento
mi
from
Sacramento, CA
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated: 12/31/1969
Eye Site Sacramento
mi
from
Sacramento, CA
Click here to add this to my saved trials
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated:  12/31/1969
East West Eye Institute
mi
from
Torrance, CA
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated: 12/31/1969
East West Eye Institute
mi
from
Torrance, CA
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ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated:  12/31/1969
Seidenberg Protzko Eye Associates
mi
from
Havre de Grace, MD
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated: 12/31/1969
Seidenberg Protzko Eye Associates
mi
from
Havre de Grace, MD
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ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated:  12/31/1969
Eye Clinics of South Texas
mi
from
San Antonio, TX
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated: 12/31/1969
Eye Clinics of South Texas
mi
from
San Antonio, TX
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ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated:  12/31/1969
R&R Research
mi
from
San Antonio, TX
ALLEVIATE Trial - A Phase 3 Trial in Subjects With Allergic Conjunctivitis
A Multi-Center, Double-Masked, Randomized, Parallel-Group, Vehicle-Controlled, Phase 3 Clinical Trial to Assess the Safety and Efficacy of Reproxalap Ophthalmic Solutions (0.25% and 0.5%) Compared to Vehicle in the Conjunctival Allergen Challenge (Ora-CAC®) Model of Acute Allergic Conjunctivitis
Status: Enrolling
Updated: 12/31/1969
R&R Research
mi
from
San Antonio, TX
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Safety/Efficacy of Nepafenac Punctal Plug Delivery System Compared to Placebo to Control Ocular Pain/Inflammation After Cataract
Clinical Study Evaluating Safety and Efficacy of a Nepafenac Punctal Plug Delivery System (N-PPDS) Compared With Placebo Punctal Plug Delivery System (p-PPDS) in Controlling Post-Operative Ocular Pain and Inflammation After Routine Unilateral Cataract Surgery
Status: Enrolling
Updated:  12/31/1969
Cincinnati Eye Institute-Edgewood
mi
from
Edgewood, KY
Safety/Efficacy of Nepafenac Punctal Plug Delivery System Compared to Placebo to Control Ocular Pain/Inflammation After Cataract
Clinical Study Evaluating Safety and Efficacy of a Nepafenac Punctal Plug Delivery System (N-PPDS) Compared With Placebo Punctal Plug Delivery System (p-PPDS) in Controlling Post-Operative Ocular Pain and Inflammation After Routine Unilateral Cataract Surgery
Status: Enrolling
Updated: 12/31/1969
Cincinnati Eye Institute-Edgewood
mi
from
Edgewood, KY
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Safety/Efficacy of Nepafenac Punctal Plug Delivery System Compared to Placebo to Control Ocular Pain/Inflammation After Cataract
Clinical Study Evaluating Safety and Efficacy of a Nepafenac Punctal Plug Delivery System (N-PPDS) Compared With Placebo Punctal Plug Delivery System (p-PPDS) in Controlling Post-Operative Ocular Pain and Inflammation After Routine Unilateral Cataract Surgery
Status: Enrolling
Updated:  12/31/1969
Ophthalmic Consultants of Long Island
mi
from
Garden City, NY
Safety/Efficacy of Nepafenac Punctal Plug Delivery System Compared to Placebo to Control Ocular Pain/Inflammation After Cataract
Clinical Study Evaluating Safety and Efficacy of a Nepafenac Punctal Plug Delivery System (N-PPDS) Compared With Placebo Punctal Plug Delivery System (p-PPDS) in Controlling Post-Operative Ocular Pain and Inflammation After Routine Unilateral Cataract Surgery
Status: Enrolling
Updated: 12/31/1969
Ophthalmic Consultants of Long Island
mi
from
Garden City, NY
Click here to add this to my saved trials
Safety/Efficacy of Nepafenac Punctal Plug Delivery System Compared to Placebo to Control Ocular Pain/Inflammation After Cataract
Clinical Study Evaluating Safety and Efficacy of a Nepafenac Punctal Plug Delivery System (N-PPDS) Compared With Placebo Punctal Plug Delivery System (p-PPDS) in Controlling Post-Operative Ocular Pain and Inflammation After Routine Unilateral Cataract Surgery
Status: Enrolling
Updated:  12/31/1969
Kerry Solomon, MD
mi
from
Mount Pleasant, SC
Safety/Efficacy of Nepafenac Punctal Plug Delivery System Compared to Placebo to Control Ocular Pain/Inflammation After Cataract
Clinical Study Evaluating Safety and Efficacy of a Nepafenac Punctal Plug Delivery System (N-PPDS) Compared With Placebo Punctal Plug Delivery System (p-PPDS) in Controlling Post-Operative Ocular Pain and Inflammation After Routine Unilateral Cataract Surgery
Status: Enrolling
Updated: 12/31/1969
Kerry Solomon, MD
mi
from
Mount Pleasant, SC
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Intravitreal Alfibercept for Center Involved DME Previously Managed With Intravitreal Ranibizumab
Efficacy of Intravitreal Aflibercept Injection (IAI) Administered in a Treat and Extend Fashion in Patients With Center Involved Diabetic Macular Edema (DME) Previously Managed With 0.3 mg Intravitreal Ranibizumab
Status: Enrolling
Updated:  12/31/1969
Charlotte Eye, Ear, Nose & Throat Associates
mi
from
Charlotte, NC
Intravitreal Alfibercept for Center Involved DME Previously Managed With Intravitreal Ranibizumab
Efficacy of Intravitreal Aflibercept Injection (IAI) Administered in a Treat and Extend Fashion in Patients With Center Involved Diabetic Macular Edema (DME) Previously Managed With 0.3 mg Intravitreal Ranibizumab
Status: Enrolling
Updated: 12/31/1969
Charlotte Eye, Ear, Nose & Throat Associates
mi
from
Charlotte, NC
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Intravitreal Alfibercept for Center Involved DME Previously Managed With Intravitreal Ranibizumab
Efficacy of Intravitreal Aflibercept Injection (IAI) Administered in a Treat and Extend Fashion in Patients With Center Involved Diabetic Macular Edema (DME) Previously Managed With 0.3 mg Intravitreal Ranibizumab
Status: Enrolling
Updated:  12/31/1969
Charlotte Eye Ear Nose & Throat Associates, P.A.
mi
from
Statesville, NC
Intravitreal Alfibercept for Center Involved DME Previously Managed With Intravitreal Ranibizumab
Efficacy of Intravitreal Aflibercept Injection (IAI) Administered in a Treat and Extend Fashion in Patients With Center Involved Diabetic Macular Edema (DME) Previously Managed With 0.3 mg Intravitreal Ranibizumab
Status: Enrolling
Updated: 12/31/1969
Charlotte Eye Ear Nose & Throat Associates, P.A.
mi
from
Statesville, NC
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The eyeGuide: Improving Glaucoma Self-management With a Personalized Behavior Change Program
The eyeGuide: Improving Glaucoma Self-management With a Personalized Behavior Change Program
Status: Enrolling
Updated:  12/31/1969
University of Michigan
mi
from
Ann Arbor, MI
The eyeGuide: Improving Glaucoma Self-management With a Personalized Behavior Change Program
The eyeGuide: Improving Glaucoma Self-management With a Personalized Behavior Change Program
Status: Enrolling
Updated: 12/31/1969
University of Michigan
mi
from
Ann Arbor, MI
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Study to Compare Kowa OCT Bi-μ and the Optovue iVue 100
Pilot Comparative Study of the Kowa OCT Bi-μ and the Optovue iVue 100
Status: Enrolling
Updated:  12/31/1969
Andover Eye Associates
mi
from
Andover, MA
Study to Compare Kowa OCT Bi-μ and the Optovue iVue 100
Pilot Comparative Study of the Kowa OCT Bi-μ and the Optovue iVue 100
Status: Enrolling
Updated: 12/31/1969
Andover Eye Associates
mi
from
Andover, MA
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Optimizing the Ocular Surface Prior to Cataract Surgery
Optimizing the Ocular Surface Prior to Cataract Surgery
Status: Enrolling
Updated:  12/31/1969
Virginia Eye Consultants
mi
from
Norfolk, VA
Optimizing the Ocular Surface Prior to Cataract Surgery
Optimizing the Ocular Surface Prior to Cataract Surgery
Status: Enrolling
Updated: 12/31/1969
Virginia Eye Consultants
mi
from
Norfolk, VA
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Safety and Efficacy of CBT-001 Ophthalmic Solution in Patients With Pterygium
A Phase 2a Multicenter, Randomized, Vehicle-Controlled, Dose Escalating Study to Evaluate the Safety, Efficacy and Pharmacokinetics of CBT-001 Ophthalmic Solution in Patients With Primary or Recurrent Pterygium
Status: Enrolling
Updated:  12/31/1969
Harvard Eye Associates
mi
from
Laguna Beach, CA
Safety and Efficacy of CBT-001 Ophthalmic Solution in Patients With Pterygium
A Phase 2a Multicenter, Randomized, Vehicle-Controlled, Dose Escalating Study to Evaluate the Safety, Efficacy and Pharmacokinetics of CBT-001 Ophthalmic Solution in Patients With Primary or Recurrent Pterygium
Status: Enrolling
Updated: 12/31/1969
Harvard Eye Associates
mi
from
Laguna Beach, CA
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Bausch & Lomb Ophthalmic Viscosurgical Device (OVD) Dispersive (DVisc40)
A Study to Document the Safety and Effectiveness of a New OVD When Compared to a Control OVD
Status: Enrolling
Updated:  12/31/1969
Valeant Site 11
mi
from
San Diego, CA
Bausch & Lomb Ophthalmic Viscosurgical Device (OVD) Dispersive (DVisc40)
A Study to Document the Safety and Effectiveness of a New OVD When Compared to a Control OVD
Status: Enrolling
Updated: 12/31/1969
Valeant Site 11
mi
from
San Diego, CA
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Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Dr. James Weber & Associates, PA
mi
from
Jacksonville, FL
Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Dr. James Weber & Associates, PA
mi
from
Jacksonville, FL
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Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Vue Optical Boutique
mi
from
Jacksonville, FL
Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Vue Optical Boutique
mi
from
Jacksonville, FL
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Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated:  12/31/1969
VisionCare Associates
mi
from
East Lansing, MI
Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated: 12/31/1969
VisionCare Associates
mi
from
East Lansing, MI
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Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Pickens Family Eye Care
mi
from
Pickens, SC
Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Pickens Family Eye Care
mi
from
Pickens, SC
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Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated:  12/31/1969
William J. Bogus, OD
mi
from
Salt Lake City, UT
Evaluation of Approved and Investigational Contact Lenses
Evaluation of Approved and Investigational Contact Lenses
Status: Enrolling
Updated: 12/31/1969
William J. Bogus, OD
mi
from
Salt Lake City, UT
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
mi
from
Brea, CA
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
mi
from
Brea, CA
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Campbell, CA
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Campbell, CA
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
mi
from
Cupertino, CA
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
mi
from
Cupertino, CA
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Mission Viejo, CA
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Mission Viejo, CA
Click here to add this to my saved trials
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Colorado Springs, CO
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Colorado Springs, CO
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Bridgeport, CT
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Bridgeport, CT
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Aventura, FL
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Aventura, FL
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Jacksonville, FL
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Jacksonville, FL
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Tallahassee, FL
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Tallahassee, FL
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Tampa, FL
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Tampa, FL
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Winter Park, FL
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Winter Park, FL
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Roswell, GA
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Roswell, GA
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Bloomington, IL
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Bloomington, IL
Click here to add this to my saved trials
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Mishawaka, IN
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Mishawaka, IN
Click here to add this to my saved trials
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Pittsburg, KA
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Pittsburg, KA
Click here to add this to my saved trials
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Boston, MA
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Boston, MA
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Independence, MO
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Independence, MO
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
mi
from
Raytown, MO
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
mi
from
Raytown, MO
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
mi
from
Closter, NJ
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
mi
from
Closter, NJ
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
New York, NY
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
New York, NY
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Raleigh, NC
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Raleigh, NC
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
mi
from
North Olmsted, OH
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
mi
from
North Olmsted, OH
Click here to add this to my saved trials
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
mi
from
Powell, OH
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
mi
from
Powell, OH
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Kittanning, PA
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Kittanning, PA
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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Warwick, RI
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Warwick, RI
Click here to add this to my saved trials
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
mi
from
Chamberlain, SD
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
mi
from
Chamberlain, SD
Click here to add this to my saved trials
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated:  12/31/1969
Clinical Research Facility
mi
from
Bartlett, TN
Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Bartlett, TN
Click here to add this to my saved trials