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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00372827
Other study ID # CM-03-06
Secondary ID
Status Completed
Phase Phase 4
First received September 6, 2006
Last updated November 18, 2016
Start date February 2004
Est. completion date January 2006

Study information

Verified date May 2008
Source Alcon Research
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

The purpose of the study is to compare the efficacy and safety of Timolol 0.5% solution to Brinzolamide 1% each given twice daily when added to Travoprost 0.004% given each evening.


Recruitment information / eligibility

Status Completed
Enrollment 245
Est. completion date January 2006
Est. primary completion date January 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients who are treated with any prostaglandin analogue monotherapy (excluding unoprostone) and who have an intraocular pressure between 19 and 32 mmHg at 08:00 hours.

Exclusion Criteria:

- Under 18 years

Study Design

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


Intervention

Drug:
Brinzolamide 1% added to Travoprost 0.004%


Locations

Country Name City State
Germany Mainz Site Mainz

Sponsors (1)

Lead Sponsor Collaborator
Alcon Research

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Holló G, Chiselita D, Petkova N, Cvenkel B, Liehneova I, Izgi B, Berta A, Szaflik J, Turacli E, Stewart WC. The efficacy and safety of timolol maleate versus brinzolamide each given twice daily added to travoprost in patients with ocular hypertension or p — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Mean diurnal intraocular pressure at month 3
Secondary Individual intraocular pressures measured at 08:00, 12:00 and 16:00 at month 3.
Secondary Reduction from baseline in mean diurnal intraocular pressure and individual timepoints.
Secondary Visual acuity, Slit lamp biomicroscopy and adverse events during 3 months.
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