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NCT00611403 · ClinicalTrials.gov registry record · Phase 2
Safety and Efficacy Study of Cyclosporine Ophthalmic Emulsion in Post-LASIK Patients
A Phase 2 study, sponsored by Allergan.
- Completed
- Registry status
- Phase 2
- Development phase
- 137
- Enrollment target
NCT00611403: Completed Phase 2 study, sponsored by Allergan.
NCT00611403 is a Phase 2 study that has completed, run by Allergan. The registered enrollment target is 137 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00611403, a Phase 2 study, has completed, sponsored by Allergan.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 137 participants
- Enrollment target
Study Summary
This study will evaluate the safety and efficacy of cyclosporine ophthalmic emulsion administered twice daily following LASIK surgery
Primary Outcome
Percentage of patients with clinical success at month 6. Clinical success is defined as the percentage of patients with corneal sensitivity (the capability of the cornea to respond to stimulation) \>= 50 millimeters in all regions of the study eye at month 6 of the Treatment Phase.
Interventions
- DRUG Cyclosporine Ophthalmic Emulsion 0.05% (RESTASIS®)
- DRUG Artificial Tears REFRESH ENDURA®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 137 participants |
| Start Date | 2007-12 |
| Est. Completion | 2009-06 |
| Phase | Phase 2 |
What the finished NCT00611403 record still lists
NCT00611403 is an interventional study that assigns participants to a tested intervention. The registered 137 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which Cyclosporine Ophthalmic Emulsion 0.05% (RESTASIS®) is the first listed.
NCT00611403 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00611403 about?
NCT00611403 is a clinical study titled "Safety and Efficacy Study of Cyclosporine Ophthalmic Emulsion in Post-LASIK Patients". This study will evaluate the safety and efficacy of cyclosporine ophthalmic emulsion administered twice daily following LASIK surgery
What is the current status of trial NCT00611403?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 137 participants. The study started on 2007-12. Estimated completion is 2009-06.
What interventions are being tested in trial NCT00611403?
The interventions under investigation include: Cyclosporine Ophthalmic Emulsion 0.05% (RESTASIS®) (DRUG), Artificial Tears REFRESH ENDURA® (DRUG).
Who is sponsoring clinical trial NCT00611403?
This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00611403's enrollment target sits among peer trials
137 527th of 2000 higher than 1,474 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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