Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Prominence

Last updated: April 5, 2013
Sponsor: Allergan
Overall Status: Completed

Phase

4

Condition

Alopecia

Hair Loss

Treatment

N/A

Clinical Study ID

NCT01448525
GMA-LTS-11-002
  • Ages 18-65
  • Female

Study Summary

The purpose of this study is to determine patient satisfaction with LATISSE® treatment for increasing eyelash prominence.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Have inadequate eyelashes

  • Never used prescription eyelash growth products

Exclusion

Exclusion Criteria:

  • No visible eyelashes

  • Permanent eyeliner or eyelash implants

  • Semi-permanent eyelash tint, dye, or extensions within 3 months

  • Over-the-counter eyelash growth products within 6 months

  • Any disease, infection or abnormality of the eye or area around the eye

  • Eye surgery within 3 months, or the anticipated need for eye surgery during the study

  • Unable or unwilling to keep contact lenses out during drug application and for 30minutes after application

Study Design

Total Participants: 88
Study Start date:
October 01, 2011
Estimated Completion Date:
April 30, 2012

Connect with a study center

  • Coral Gables, Florida
    United States

    Site Not Available

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