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NCT00370201 Clinical Trial

Efficacy of Oral Colchicine in Prevention of Proliferative Vitreoretinopathy in Rhegmatogenous Retinal Detachment

Rhegmatogenous Retinal Detachment Clinical Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00370201
Other study ID # 8259
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received August 30, 2006
Last updated October 6, 2006
Start date March 2004
Est. completion date August 2006

Study information
Verified date March 2004
Source hahid Beheshti University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

This clinical trial will test the efficacy and safety of oral colchicine in prevention of proliferative vitreoretinopathy (PVR) in cases of rhegmatogenous retinal detachment

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 0
Est. completion date August 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Rhegmatogenous retinal detachment

Exclusion Criteria:

- PVR grade C

- Duration of retinal detachment = one month

- History of cataract surgery

- History of RD surgery

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• colchicine

Locations
Country Name City State
Iran, Islamic Republic of Hamid Ahmadieh,MD Tehran

Sponsors (1)
Lead Sponsor Collaborator
hahid Beheshti University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary proliferative vitreoretinopathy
Primary retinal reattachment rate
Secondary visual acuity
Secondary reoperation
Secondary macular pucker
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