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N/A N=45 Randomized Quadruple-blind Treatment

Cutaneous Prostaglandin Application: Nail Growth, Nail Brittleness, and Eye Pressure

Nail Growth Cessation · Intraocular Pressure

Enrolled (actual)
45
Serious AEs
0.0%
Results posted
Dec 2019
Primary outcome: Primary: Change From Baseline in Nail Length of Hands — 13.49; 15.10; 1.34; 1.51 mm — p=0.532

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Bimatoprost 0.01% (Drug); Placebo: saline (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Northwestern University
Primary completion
May 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Nail Length of Hands
13.49; 15.10; 1.34; 1.51 0.532
PRIMARY
Change From Baseline in Nail Length of Digits
1.58; 1.48; 1.26; 1.02; 0.90; 1.40 0.523
PRIMARY
Intraocular Pressure at 30 Days of Treatment
16.42; 13.91; 16.38; 14.0; 16.46; 13.82 0.912
PRIMARY
Nail Brittleness at 30 Days of Treatment
2.25; 2.43 0.062
SECONDARY
Number of Days Until the First Nail Chipped
8.38; 6.26
SECONDARY
Change in Skin Pigmentation on Hands
10; 0; 19; 30; 1; 0
SECONDARY
Change in Hirsutism on Hands
0; 0; 34; 34; 0; 0

Summary

Topical prostaglandin agents are used to help reduce eye pressure in glaucoma patients. Bimatoprost (Lumigan 0.01%) is such an agent (Allergan, Inc.). Several of our patients on bimatoprost and an observational study of patients on bimatoprost in another center reported that fingernails grew longer and became less brittle using the topical eye drops to the eyes. The purpose of the double-blinded study is to determine whether the application of the eye drops directly to the proximal nail fold of one hand using the opposite hand as a control will result in longer nails, less brittle nails, and reduced eye pressures should any of the medication be absorbed into the systemic circulation.

Eligibility Criteria

Inclusion Criteria

  • English speaking
  • Normotensive or glaucoma suspects on no ocular medications
  • No manicure within 2 weeks of the study.

Exclusion Criteria

  • Individuals on topical or systemic essential fatty acids (EFA's) in hand lotions, creams, ointments, or medication, or on biotin.
  • Digits with signs of nail injury, deformity, or infection.
  • Nail biters, nail polishers, artificial nail wear or gels, and nail and trimming and filing until the study endpoint.
  • Women of childbearing age who are pregnant or who are trying to become pregnant.
  • Individuals with allergies or sensitivity to prostaglandin agents.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02448043). 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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