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N/A N=21 Triple-blind Treatment

Eyelash Growth From Application of Bimatoprost in Gel Suspension to the Base of the Eyelashes

Hypertrichosis

Enrolled (actual)
21
Serious AEs
0.0%
Results posted
Apr 2014
Primary outcome: Primary: Efficacy of Bimatoprost in Lengthening of Eyelashes — 2; 1.1 mm

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Bimatoprost Suspension (Drug)
Age
Adult, Older Adult · 20+ yrs
Sex
All
Sponsor
University of Miami
Primary completion
Jul 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Efficacy of Bimatoprost in Lengthening of Eyelashes
2; 1.1

Summary

Objective: To determine if Lumigan (bimatoprost) causes increased lash length when used in gel suspension applied to the base of the eyelashes. Methods: Subjects recruited from the Bascom Palmer Eye Institute were screened and those who met inclusion criteria were enrolled. Each participant received two vials of gel suspension, which contained bimatoprost and normal saline, respectively, each mixed 1:1 with GonakTM gel and labeled "right eye" and "left eye" according to randomization. The suspension was applied to the eyelashes every evening on the designated eye for 6 weeks. Lash length was measured with a caliper at enrollment, at weekly intervals during the study and at 1 and 3 months after study completion. Visual acuity, ocular symptoms, intraocular pressure and photographs were documented at these same intervals. Results: The average eyelash growth in the Lumigan group was 2.01mm (vs. control average of 1.13mm) which was a statistically significant difference (p=0.009). The average intraocular pressure decreased equally in both groups (2.14 mmHg). No change in visual acuity or iris discoloration was noted in any of the subjects. Discussion: Our data showed an increase in eyelash length with use of Lumigan in gel suspension, suggesting that it may have eyelash lengthening properties.

Eligibility Criteria

Inclusion Criteria

  • Age greater than 20 and less than 90 and patients who have previously used and are comfortable with applying mascara.

Exclusion Criteria

  • History of glaucoma, uveitis, pregnancy, allergic reaction to prostaglandins or the gel suspension, alopecia, and previous usage of other eyelash growth enhancement.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00773136). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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