Clinical Trials Directory

Trials / Completed

CompletedNCT01391273

Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypotrichosis

A Multicenter, Double-masked, Randomized, Parallel-group Study Assessing the Safety and Efficacy of Once-Daily Application of Bimatoprost Solution 0.03% Compared to Vehicle in Increasing Overall Eyelash Prominence in Japanese Subjects With Hypotrichosis of the Eyelashes

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
173 (actual)
Sponsor
Allergan · Industry
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate the safety and efficacy of bimatoprost solution 0.03% compared with vehicle in Japanese adults with hypotrichosis of the eyelashes.

Conditions

Interventions

TypeNameDescription
DRUGbimatoprost solution 0.03%One drop of bimatoprost solution 0.03% applied along each upper eyelid margin once daily in the evening for 4 months.
DRUGbimatoprost vehicle solutionOne drop of bimatoprost vehicle solution applied along each upper eyelid margin once daily in the evening for 4 months.

Timeline

Start date
2011-07-01
Primary completion
2012-05-19
Completion
2012-05-19
First posted
2011-07-12
Last updated
2019-07-08
Results posted
2013-07-09

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT01391273. Inclusion in this directory is not an endorsement.