Expired Study
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West Palm Beach, Florida 33401


Purpose:

The primary purpose of this study is to assess efficacy and safety of Latisse (bimatoprost .03% ophthalmic solution) applied to the lateral and medial eyebrows. The primary outcome is a increase in overall eyebrow prominence as measured by at least a 1-grade increase on the Global Eyebrow Assessment (GEyA) scale, from baseline to the end of the treatment which will be day 270 period.


Criteria:

Inclusion Criteria: - Outpatient, female/male subjects of any race, 18-75 years of age. - Subjects of childbearing potential must have a negative urine pregnancy test result at Baseline and practice a reliable method of contraception throughout the study - Patients with hypotrichosis (thinning) of the eyebrows with a GEyA score of 1 or 2. - Patient agrees to abstain from any treatment to the eyebrows including: waxing, plucking, threading, laser hair removal, and/or bleaching (excluding the glabella region). - Able to understand the requirements of the study and sign Informed Consent/HIPAA Authorization forms. - Written informed consent and written authorization for use or release of health and research information obtained. - Willing to complete all required study visits, procedures, and evaluations including photography. Exclusion Criteria: - Subjects who are pregnant (positive urine pregnancy test), planning to become pregnant, breast-feeding, or who are of childbearing potential and not practicing a reliable method of birth control. - Patients with any uncontrolled systemic disease - Patient with any known disease or abnormality of the eyebrows including eczema and seborrheic dermatitis - Patients with known or suspected trichotillomania disorder - Patients with a history of glaucoma and/or increased ocular pressure - Patients who are currently using an IOP-lowering prostaglandin analog (including Lumigan) - Patients with a known hypersensitivity to bimatoprost or any other ingredient in Latisse - Previous cosmetic surgery to the upper face (e.g., periorbital surgery, brow lift, eyelid or eyebrow surgery, etc.). - Patients with permanent eye and/or eyebrow make-up - Any eyebrow tint or dye applications within 2 months prior to study entry - Any planned facial cosmetic procedure that would interfere with the evaluation of the eyebrows - Participation in another investigational drug or device study within the last 30 days


NCT ID:

NCT01387906


Primary Contact:

Principal Investigator
Kenneth Beer, M.D.
Beer, Kenneth R., M.D., PA


Backup Contact:

N/A


Location Contact:

West Palm Beach, Florida 33401
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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