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NCT00991458 · ClinicalTrials.gov registry record · Phase 2

Study of Cyclosporine in Post-LASIK Patients

A Phase 2 study, sponsored by Allergan.

Completed
Registry status
Phase 2
Development phase
621
Enrollment target

NCT00991458: Completed Phase 2 study, sponsored by Allergan.

NCT00991458 is a Phase 2 study that has completed, run by Allergan. The registered enrollment target is 621 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (367% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00991458, a Phase 2 study, has completed, sponsored by Allergan.

COMPLETED
Registry status
Phase 2
Development phase
621 participants
Enrollment target

Study Summary

This study will evaluate the safety and efficacy of Cyclosporine 0.005% and 0.010% eye drops administered twice daily before and following LASIK surgery.

Primary Outcome

Time to cure is defined as the number of days after laser in situ keratomileusis (LASIK) surgery that the patient has corneal sensitivity (the capability of the cornea to respond to stimulation) ≥ 50 millimeters in all 9 regions of both eyes after LASIK surgery. A patient is considered cured at the first of 2 consecutive visits meeting these criteria. The Inter-Quartile Range presented is actually the 25th Quantile and the 75th Quantile obtained from the Kaplan-Meier Model.

Interventions

  • DRUG Cyclosporine 0.010% eye drops
  • DRUG Cyclosporine 0.005% eye drops
  • DRUG Placebo (Vehicle for Cyclosporine)

Trial Details

FieldValue
Enrollment Target 621 participants
Start Date 2009-10
Est. Completion 2011-04
Phase Phase 2
Allergan

314 total trials

What the finished NCT00991458 record still lists

NCT00991458 is an interventional study that assigns participants to a tested intervention. The registered 621 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (367% higher).

The record links to 0 conditions, and to 3 interventions - of which Cyclosporine 0.010% eye drops is the first listed.

NCT00991458 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00991458 about?

NCT00991458 is a clinical study titled "Study of Cyclosporine in Post-LASIK Patients". This study will evaluate the safety and efficacy of Cyclosporine 0.005% and 0.010% eye drops administered twice daily before and following LASIK surgery.

What is the current status of trial NCT00991458?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 621 participants. The study started on 2009-10. Estimated completion is 2011-04.

What interventions are being tested in trial NCT00991458?

The interventions under investigation include: Cyclosporine 0.010% eye drops (DRUG), Cyclosporine 0.005% eye drops (DRUG), Placebo (Vehicle for Cyclosporine) (DRUG).

Who is sponsoring clinical trial NCT00991458?

This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00991458's enrollment target sits among peer trials

621 52nd of 2000 higher than 1,949 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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Source: ClinicalTrials.gov NCT00991458, the US trial registry maintained by the National Library of Medicine. NCT00991458 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.