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Clinical Trial Summary

This one-year study evaluates the long-term safety and effectiveness of bimatoprost solution application to the eyelid margin (where the eyelashes meet the skin) to treat hypotrichosis of the eyelashes (inadequate or not enough eyelashes). There will be two different types of subjects participating in the study 1)those with inadequate eyelashes due to natural causes or 2) those with inadequate eyelashes following a complete course of chemotherapy treatment. There will be two treatment periods of six months each. Subjects will receive either the study medication or vehicle in either of the two treatment periods.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00907426
Study type Interventional
Source Allergan
Contact
Status Completed
Phase Phase 3
Start date August 2009
Completion date May 2011

See also
  Status Clinical Trial Phase
Completed NCT01448525 - Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Prominence Phase 4
Completed NCT00958035 - Study of Bimatoprost Solution in Increasing Eyelash Prominence in African Americans With Eyelash Hypotrichosis Phase 4
Completed NCT01891487 - Safety and Efficacy of Bimatoprost 0.03% Solution for the Treatment of Thinning Eyebrows Phase 4
Completed NCT01387906 - Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosis of the Eyebrows: Latisse Versus Placebo Phase 4
Recruiting NCT05790941 - Proof of Concept Study of Latanoprost/Minoxidil (ANR-001.1) Topical Formulation Early Phase 1
Recruiting NCT05723198 - A Study of Baricitinib (LY3009104) in Children From 6 Years to Less Than 18 Years of Age With Alopecia Areata Phase 3
Completed NCT01200251 - Study of Bimatoprost Gel on Eyelash Growth Phase 3