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NCT00828906 Clinical Trial

DuoTrav® Eye Drops As Replacement Therapy Program

Ocular Hypertension Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00828906
Other study ID # DART-2
Secondary ID
Status Completed
Phase Phase 4
First received January 23, 2009
Last updated September 18, 2012
Start date February 2009

Study information
Verified date July 2012
Source Alcon Research
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Interventional

Clinical Trial Summary

To evaluate the effectiveness of DuoTrav Eye Drops in gaining or maintaining control of target Intraocular Pressures (tIOP) in patients diagnosed with, and being treated for, open-angle glaucoma (OAG) or ocular hypertension (OH).

Recruitment information / eligibility
Status Completed
Enrollment 128
Est. completion date
Est. primary completion date November 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with OAG or OH for whom single agent therapy provides insufficient intraocular pressure reduction

Exclusion Criteria:

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• DuoTrav
DuoTrav Eye Drops

Locations
Country Name City State
China Contact Alcon for Trial Locations Bejing

Sponsors (1)
Lead Sponsor Collaborator
Alcon Research

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Intra Ocular Pressure visit 1, Visits 2-3, Visits 6-8 No
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