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Clinical Trials/NCT00825396
NCT00825396
Completed
Not Applicable

A Pilot, Open-Label, Controlled Clinical Trial of C-KAD Ophthalmic Solution in Reducing Intraocular Pressure in Patients With Ocular Hypertension

Chakshu Research, Inc.1 site in 1 country12 target enrollmentApril 2007

Overview

Phase
Not Applicable
Intervention
C-KAD Ophthalmic Solution
Conditions
Ocular Hypertension
Sponsor
Chakshu Research, Inc.
Enrollment
12
Locations
1
Primary Endpoint
Mean change in intraocular pressure from baseline
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The purpose of this study is to determine the safety and tolerability of topical C-KAD Ophthalmic Solution in reducing intraocular pressure in patients with ocular hypertension.

Registry
clinicaltrials.gov
Start Date
April 2007
End Date
April 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Both eyes having intraocular pressure in the range of 22-30 mmHg at baseline
  • Both eyes having best corrected visual acuity better than 20/50

Exclusion Criteria

  • Advanced glaucoma
  • Closed or barely open anterior chamber or history of angle closure

Arms & Interventions

C-KAD Ophthalmic Solution

Intervention: C-KAD Ophthalmic Solution

Outcomes

Primary Outcomes

Mean change in intraocular pressure from baseline

Time Frame: 150 Days

Study Sites (1)

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