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NCT01189747 · ClinicalTrials.gov registry record · Phase 3
Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's Feet Lines
A Phase 3 study, sponsored by Allergan.
- Completed
- Registry status
- Phase 3
- Development phase
- 446
- Enrollment target
NCT01189747 is a Phase 3 study that has completed, run by Allergan. The registered enrollment target is 446 participants.
The verdict
NCT01189747, a Phase 3 study, has completed, sponsored by Allergan.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 446 participants
- Enrollment target
Study Summary
This study will evaluate the safety and efficacy of botulinum toxin Type A compared to placebo for the treatment of Crow's Feet Lines (Lateral Canthal Rhytides).
Interventions
- DRUG normal saline
- BIOLOGICAL onabotulinumtoxinA
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 446 participants |
| Start Date | 2010-10-01 |
| Est. Completion | 2011-07-01 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01189747
The ClinicalTrials.gov registry entry for NCT01189747 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 446 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Allergan, which has 314 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which normal saline is the first listed.
NCT01189747 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01189747 about?
NCT01189747 is a clinical study titled "Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's Feet Lines". This study will evaluate the safety and efficacy of botulinum toxin Type A compared to placebo for the treatment of Crow's Feet Lines (Lateral Canthal Rhytides).
What is the current status of trial NCT01189747?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 446 participants. The study started on 2010-10-01. Estimated completion is 2011-07-01.
What interventions are being tested in trial NCT01189747?
The interventions under investigation include: normal saline (DRUG), onabotulinumtoxinA (BIOLOGICAL).
Who is sponsoring clinical trial NCT01189747?
This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.
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