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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00441181
Other study ID # UNIFESP 2007-02
Secondary ID
Status Withdrawn
Phase N/A
First received February 27, 2007
Last updated June 21, 2011
Start date January 2008
Est. completion date December 2008

Study information

Verified date February 2007
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: National Health Surveillance Agency
Study type Interventional

Clinical Trial Summary

Prostaglandin analogues have not been used in the treatment of neovascular glaucoma because of suspicious lack of efficacy. This study aims at assessing the effect of travoprost on neovascular glaucoma.


Recruitment information / eligibility

Status Withdrawn
Enrollment 40
Est. completion date December 2008
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Neovascular glaucoma of known cause

- Older than 18 years

- Previously submitted to retinal photocoagulation

- Under medical treatment to glaucoma

Exclusion Criteria:

- Need of antiglaucomatous surgery

- Previous ocular surgery in the last 6 months

- Pregnancy

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:
Travoprost


Locations

Country Name City State
Brazil Federal University of São Paulo São Paulo

Sponsors (1)

Lead Sponsor Collaborator
Federal University of São Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intraocular pressure
Secondary Inflammation
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