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

NCT ID: NCT00370201

Last Updated: 2006-10-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE3

Study Classification

INTERVENTIONAL

Study Start Date

2004-03-31

Study Completion Date

2006-08-31

Brief Summary

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

Detailed Description

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Conditions

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Rhegmatogenous Retinal Detachment

Keywords

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retinal detachment proliferative vitreoretinopathy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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colchicine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Rhegmatogenous retinal detachment

Exclusion Criteria

* PVR grade C
* Duration of retinal detachment ≥ one month
* History of cataract surgery
* History of RD surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shahid Beheshti University of Medical Sciences

OTHER

Sponsor Role lead

Principal Investigators

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Hamid Ahmadieh, MD

Role: PRINCIPAL_INVESTIGATOR

Ophthalmic Research Center of Shaheed Beheshti Medical University

Locations

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Hamid Ahmadieh,MD

Tehran, Tehran Province, Iran

Site Status

Countries

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Iran

Other Identifiers

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8259

Identifier Type: -

Identifier Source: org_study_id