Clinical Trials Directory

Trials / Completed

CompletedNCT00986427

Restasis for Treatment of Brittle Nails

Restasis® Ophthalmic Emulsion for the Treatment of Brittle Nails

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Julian M. Mackay-Wiggan · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

This purpose of this study is to assess the safety and effectiveness of Restasis® ophthalmic emulsion versus emulsion alone( Refresh Dry Eye therapy) both for the treatment of brittle nails and for the enhancement of normal nail growth and texture. The investigators think that daily application of Restasis® to nails and nail beds in patients with brittle nails will enhance nail growth and improve nail texture in both affected and unaffected nails.

Detailed description

This is a single center, investigator-blinded (investigator masked), head to head comparison of Restasis® and its vehicle, Refresh® Dry Eye Therapy in 24 patients. Three target fingernails will be identified in each subject. Two of the target nails will be the two nails that have the most severe signs of brittle nail syndrome. The third target nail will be a normal nail or, in the absence of a normal nail, the patient's second-healthiest appearing nail. The patients most normal-appearing nail will be untreated so that growth in the treated nails can be compared to growth in an untreated normal nail, this will be the fourth target nail. Study medication will be applied to target nails (the subjects may also apply to all nails if they wish, except one nail which will be untreated in order to determine the subject's baseline rate of fingernail growth) for 24 weeks. The target nails will be assessed at each visit, every four weeks. There will be a 12-week follow up period after treatment is completed. This 36 week study will be conducted at one center. Adult male and female patients meeting the inclusion and exclusion criteria will be screened for eligibility. The principal investigator or his/her designee will obtain informed consent from all patients before any protocol specific procedures are performed.

Conditions

Interventions

TypeNameDescription
DRUGRestasis (cyclosporine ophthalmic emulsion) 0.05%cyclosporine ophthalmic emulsion 0.05%
DRUGRefresh® Dry Eye therapyEmulsion contains glycerin 1% and polysorbate 80

Timeline

Start date
2009-07-01
Primary completion
2010-07-01
Completion
2012-12-01
First posted
2009-09-30
Last updated
2013-08-20
Results posted
2013-08-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00986427. Inclusion in this directory is not an endorsement.