Analysis of Impact of KeryFlex on Quality of Life for Retronychia or Lichen Planus Adult Patients

Sex: All

Ages: 18 Years – 95 Years

Healthy volunteers: 1

Phase: NA

Enrollment: 10

Sponsor: Weill Medical College of Cornell University

Summary

The purpose of this study is to assess the overall effect of KeryFlex study intervention on quality of life and functionality for patients with retronychia or nail lichen planus.

Eligibility Criteria

Inclusion criteria:Diagnosis of retronychia or nail lichen planusAble to understand and voluntarily sign an informed consent form18-95 years old at time of consentAble to adhere to the study visit schedule and other protocol requirementsExclusion criteria:Unable to provide written informed consent for any reasonDiagnosis of peripheral vascular disease, arterial insufficiency, peripheral neuropathy, suspicious pigmented lesions on the nail or in-grown nailsSensitive or allergic to any KeryFlex ingredientsUnable to abstain from using nail polishes, nail gels, or any other nail products 2 days prior to KeryFlex procedure and during the study periodPregnant, planning pregnancy, or nursing

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05699499). StuddyBuddy aggregates publicly available trial information.