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Clinical Trial Summary

A internally controlled, single-blinded, randomized controlled trial to investigate the use of Bimatoprost eyelash gel on eyelash growth and appearance in breast cancer patients who suffer from madarosis (loss of eyelashes) due to the side effects of chemotherapy. IND and IRB approval have been obtained.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01200251
Study type Interventional
Source Duke University
Contact
Status Completed
Phase Phase 3
Start date February 2007
Completion date December 2008

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 NCT00907426 - Safety and Efficacy Study of Bimatoprost to Treat Hypotrichosis of the Eyelashes After Application to the Eyelid Margin Phase 3