Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Prominence

Completed · Phase 4

Conditions studied: Hypotrichosis

In brief

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

Key facts

Study ID

NCT01448525

Run by

Allergan

People needed

88

Starts

2011-10-01

Expected to finish

2012-04-01

Last updated by the study team

2013-05-22

Who can join

Age: 18 and older, up to 65. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Have inadequate eyelashes
• Never used prescription eyelash growth products

You may not qualify if…

• 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 30 minutes after application

Where it is running

• Study site — Coral Gables, Florida, United States

Full record on ClinicalTrials.gov

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