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Clinical Trials/NCT00793091
NCT00793091
Unknown
Phase 2

A Phase 2, Randomized, Placebo-Controlled, Double-Masked, Multicenter Safety and Efficacy Study of C-KAD Ophthalmic Solution in Patients With Loss of Visual Acuity Due to Age-Related Cataract

Chakshu Research, Inc.4 sites in 1 country80 target enrollmentNovember 2008

Overview

Phase
Phase 2
Intervention
C-KAD Ophthalmic Solution
Conditions
Cataract
Sponsor
Chakshu Research, Inc.
Enrollment
80
Locations
4
Primary Endpoint
Best-corrected visual acuity by ETDRS
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is to determine the safety and efficacy of C-KAD Ophthalmic Solution in improving visual acuity relative to placebo in patients with age-related cataract

Registry
clinicaltrials.gov
Start Date
November 2008
End Date
September 2009
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Presence of age-related cataract in the study eye
  • Best-corrected visual acuity of 20/25 to 20/50 in the study eye

Exclusion Criteria

  • Any other clinical condition in the eye that may compromise vision
  • Presence or History of Glaucoma
  • Presence or history of diabetes
  • Use of eyedrops
  • Use of steroids

Arms & Interventions

1

Intervention: C-KAD Ophthalmic Solution

2

Intervention: Placebo

Outcomes

Primary Outcomes

Best-corrected visual acuity by ETDRS

Time Frame: 120 Days

Study Sites (4)

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