Topical Cyclosporine Suspension for the Treatment of Brittle Nails

Completed · Phase 2

Conditions studied: Brittle Nail Syndrome

In brief

Brittle nail syndrome (BNS) refers to nails that exhibit splitting, raggedness (fraying of the distal edge), and peeling (lamellar onychoschizia).(1) This is a common problem, affecting approximately 20% of women, with higher prevalence among the elderly.(2) A number of factors have been proposed as possible causes of nail brittleness, such as anemia, biotin deficiency, or cysteine deficiency. (3,4) However, most authors believe that brittle nails are usually caused by dehydration of the nail plate, either from repetitive cycles of hydration and dehydration related to hand washing or from exposure to dehydrating chemicals, such as those found in nail enamel and cuticle removers. (5,6) Inflammation of the nail as a potential contributing factor has never been studied. There are currently not consistently effective treatments for this condition. Restasis® is effective in treating keratoconjunctivitis sicca. This condition is characterized by the troublesome condition of dry eyes partially due to decreased tear production exacerbated by inflammation. The BNS manifests itself by nail plate dehydration. The two conditions have in common disruption of water balance which gives rise to problematic clinical disorders. The hypothesis is that a product which benefits tear production would also be effective for brittle nails which contain roughly 15% water.

Key facts

Study ID

NCT01064830

Run by

University of North Carolina, Chapel Hill

People needed

21

Starts

2010-02-01

Expected to finish

2011-08-01

Last updated by the study team

2017-03-13

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• • Must understand and voluntarily sign an informed consent form
• Must be male or female and aged 18-75 years at time of consent
• Must be able to adhere to the study visit schedule and other protocol requirements
• At least 2 of the following: raggedness (fraying of the distal edge), splitting, and peeling (lamellar onychoschizia) of 2 target fingernails of the same hand. If the subject does not have 2 fingernails affected in the same hand, a second fingernail on the other hand may be used as control.
• A direct microscopic examination with potassium hydroxide (KOH)/calcofluor that is negative for hyphae associated with dermatophytes
• Women of childbearing potential must have a negative pregnancy test at enrollment

You may not qualify if…

• Inability to provide voluntary consent
• Pregnant or breastfeeding
• Fingernail fungal infection
• Use of any investigational medication within 4 weeks prior to start of study drug
• Subject has any known immunodeficiency or history of malignancy in the last 4 years, excluding nonmelanoma skin cancer.
• Use of any topical nail medication for 2 weeks
• Use of any topical nail product (nail polish, hardeners, acetone, etc) for 1 week prior to and during the study.
• Use of biotin 2 weeks before enrollment.
• No genetic nail abnormalities
• Known sensitivity to Restasis® or RDET®.
• Subject has psoriasis, lichen planus, or other abnormalities that could result in a clinically abnormal fingernail

Where it is running

• University of North Carolina — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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