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NCT00567983 Clinical Trial

Topical Cyclosporine and Disease Progression

Disease Progression Clinical Trial

Official title:
Topical Cyclosporine and Disease Progression

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00567983
Other study ID # 13717A
Secondary ID
Status Completed
Phase Phase 4
First received December 3, 2007
Last updated September 23, 2008
Start date December 2007
Est. completion date September 2008

Study information
Verified date September 2008
Source Innovative Medical
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect Restasis has in regards to disease progression.

Recruitment information / eligibility
Status Completed
Enrollment 80
Est. completion date September 2008
Est. primary completion date September 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Mild to Moderate dry eye symptoms

Exclusion Criteria:

- Current use of Restasis

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Restasis
Restasis- (in the eye) Instill one drop twice daily Endura- (in the eye) Instill one drop twice daily
• Endura
Restasis- (in the eye) Instill one drop twice daily Endura- (in the eye) Instill one drop twice daily

Locations
Country Name City State
United States Lakeside Eye Clinic Chicago Illinois

Sponsors (1)
Lead Sponsor Collaborator
Innovative Medical

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Disease Severity 1 yr No
Secondary Staining 1 yr No
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