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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01092273
Other study ID # Prostaglandins-Cairo-1A
Secondary ID
Status Completed
Phase N/A
First received March 23, 2010
Last updated March 23, 2010

Study information

Verified date January 2008
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority Egypt:Al Nour Eye Hospital Medical Committee
Study type Observational

Clinical Trial Summary

Bimatoprost has been shown to provide effective IOP lowering in patients of all races. Conversely, travoprost has been shown to be more effective in black patients than in Caucasians in some studies. However, Noecker et al 2004 compared bimatoprost with travoprost in African-Americans with glaucoma or OHT, and found that bimatoprost was more likely than travoprost to achieve target pressure at 3 months.

These racial differences in efficacy of these medications warrant further investigations. The investigators study aim to compare the IOP-lowering efficacies of bimatoprost and travoprost in an Egyptian population with primary open-angle glaucoma (OAG) or ocular hypertension (OHT).


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 20 Years to 72 Years
Eligibility Inclusion Criteria:

- Glaucoma and Ocular Hypertension

Exclusion Criteria:

- Any ocular disease or medication that may raise the intraocular pressure.

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of intraocular pressure lowering of bimatoprost versus travoprost.
Secondary Rate of development of complications.
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