Trials / Completed
CompletedNCT00757835
24-hr IOP With Travoprost/Timolol Compared With Latanoprost/Timolol in XFG
24-hour IOP Control With the Travoprost/Timolol Fixed Combination Compared With the Latanoprost/Timolol Fixed Combination, When Both Are Dosed in the Evening in Patients With Exfoliative Glaucoma
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Aristotle University Of Thessaloniki · Academic / Other
- Sex
- All
- Age
- 21 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
A crossover, randomized, single-masked study which compares the short-term (3 months) 24-hour IOP control and safety of travoprost/timolol fixed combination given once in the evening, versus that of latanoprost/timolol fixed combination given once in the evening in patients with exfoliative glaucoma. The primary objective of this trial is to compare the quality of 24-hour IOP control after 3 months of chronic therapy with these two medications.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | treatment with latanoprost/timolol fixed combination | dosing in the evening with the two fixed combinations |
| DRUG | latanoprost/timolol fixed combination drops | once in the evening |
Timeline
- Start date
- 2008-05-01
- Primary completion
- 2009-03-01
- Completion
- 2009-03-01
- First posted
- 2008-09-23
- Last updated
- 2020-12-17
Source: ClinicalTrials.gov record NCT00757835. Inclusion in this directory is not an endorsement.