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NCT01271686 · ClinicalTrials.gov registry record · Phase 4
24-hour IOP-lowering Effect of 0.01% Bimatoprost
A Phase 4 study, sponsored by University of California, San Diego.
- Completed
- Registry status
- Phase 4
- Development phase
- 16
- Enrollment target
NCT01271686: Completed Phase 4 study, sponsored by University of California, San Diego.
NCT01271686 is a Phase 4 study that has completed, run by University of California, San Diego. The registered enrollment target is 16 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01271686, a Phase 4 study, has completed, sponsored by University of California, San Diego.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 16 participants
- Enrollment target
Study Summary
This study will evaluate the 24-hour IOP-lowering efficacy of 0.01% bimatoprost once daily in patients with glaucoma or ocular hypertension
Primary Outcome
Nocturnal IOP means under bimatoprost 0.01% treatment were compared with baseline.
Interventions
- DRUG 0.01% bimatoprost
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 16 participants |
| Start Date | 2011-01 |
| Est. Completion | 2012-10 |
| Phase | Phase 4 |
What the finished NCT01271686 record still lists
NCT01271686 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 1 intervention - of which 0.01% bimatoprost is the first listed.
NCT01271686 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01271686 about?
NCT01271686 is a clinical study titled "24-hour IOP-lowering Effect of 0.01% Bimatoprost". This study will evaluate the 24-hour IOP-lowering efficacy of 0.01% bimatoprost once daily in patients with glaucoma or ocular hypertension
What is the current status of trial NCT01271686?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 16 participants. The study started on 2011-01. Estimated completion is 2012-10.
What interventions are being tested in trial NCT01271686?
The interventions under investigation include: 0.01% bimatoprost (DRUG).
Who is sponsoring clinical trial NCT01271686?
This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01271686's enrollment target sits among peer trials
16 1869th of 2000 higher than 121 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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