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NCT00693420 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy of Bimatoprost Solution in Increasing Overall Eyelash Prominence

A Phase 3 study, sponsored by Allergan.

Completed
Registry status
Phase 3
Development phase
278
Enrollment target

NCT00693420: Completed Phase 3 study, sponsored by Allergan.

NCT00693420 is a Phase 3 study that has completed, run by Allergan. The registered enrollment target is 278 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (64% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00693420, a Phase 3 study, has completed, sponsored by Allergan.

COMPLETED
Registry status
Phase 3
Development phase
278 participants
Enrollment target

Study Summary

This study evaluates the safety and effectiveness of topical bimatoprost solution for enhancing eyelash prominence.

Primary Outcome

The GEA scale is an investigator-graded 4-point ordinal scale of overall eyelash prominence (1 \[minimal\], 2 \[moderate\], 3 \[marked\], 4 \[very marked\])

Interventions

  • DRUG Bimatoprost 0.03% sterile solution
  • DRUG vehicle sterile solution

Trial Details

FieldValue
Enrollment Target 278 participants
Start Date 2007-04
Est. Completion 2007-12
Phase Phase 3
Allergan

314 total trials

What the finished NCT00693420 record still lists

NCT00693420 is an interventional study that assigns participants to a tested intervention. The registered 278 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (64% lower).

The record links to 0 conditions, and to 2 interventions - of which Bimatoprost 0.03% sterile solution is the first listed.

NCT00693420 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00693420 about?

NCT00693420 is a clinical study titled "Safety and Efficacy of Bimatoprost Solution in Increasing Overall Eyelash Prominence". This study evaluates the safety and effectiveness of topical bimatoprost solution for enhancing eyelash prominence.

What is the current status of trial NCT00693420?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 278 participants. The study started on 2007-04. Estimated completion is 2007-12.

What interventions are being tested in trial NCT00693420?

The interventions under investigation include: Bimatoprost 0.03% sterile solution (DRUG), vehicle sterile solution (DRUG).

Who is sponsoring clinical trial NCT00693420?

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

How this trial's enrollment target compares

Where NCT00693420's enrollment target sits among peer trials

278 1200th of 2000 higher than 799 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT00693420, the US trial registry maintained by the National Library of Medicine. NCT00693420 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.