ClinConnect ClinConnect Logo
Search / Trial NCT02797574

Stress Response Pathways in Vitiligo

Launched by NYU LANGONE HEALTH · Jun 8, 2016

Trial Information

Current as of April 29, 2025

Completed

Keywords

ClinConnect Summary

Identifying a role for NF-κB signaling in vitiligo may improve therapies for this disfiguring disorder. Current treatments vary in effectiveness and may not always be long lasting cases. The NF-κB pathway and IL-6 itself are the target of several FDA approved drugs, thus opening new therapeutic avenues.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • * To be eligible for participation, subjects must meet all of the following criteria:
  • Must have a clinical exam consistent with and diagnosis of non-segmental vitiligo
  • Must be normally pigmented
  • No clinical presentation of vitiligo
  • Exclusion Criteria:
  • Outside of the specified age range
  • No clinical diagnosis of vitiligo
  • Use of systemic therapies, including but not limited to methotrexate, etretinate, or cyclosporine, calcineurin inhibitors and/ or vitamin D analogs within 4 weeks of enrollment
  • Use of topical steroids or topical immunodilators at biopsy site within 4 weeks of enrollment
  • History of keloids or hypertrophic scars
  • Patients with pacemakers or defibrillators or heart valves
  • Patients on Plavix, Warfarin or similar anticoagulation medicine
  • Pregnant females
  • Lactating women
  • Allergies or sensitivity to lidocaine or epinephrine
  • Outside of the specified age range
  • Abnormally pigmented at potential biopsy sites (non-vitiligo)
  • Clinical presentation of vitiligo
  • Use of systemic therapies, including but not limited to methotrexate, etretinate, or cyclosporine, calcineuron inhibitors and/ or vitamin D analogs within 4 weeks of enrollment
  • Use of topical steroids or topical immunodilators at biopsy site within 4 weeks of enrollment
  • History of keloids or hypertrophic scars

About Nyu Langone Health

NYU Langone Health is a premier academic medical center located in New York City, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. As a leading sponsor of clinical trials, NYU Langone Health integrates cutting-edge scientific inquiry with patient-centered care, striving to develop new therapies and improve health outcomes across a wide range of medical conditions. The institution is dedicated to fostering collaboration among researchers, clinicians, and patients, ensuring rigorous adherence to ethical standards and regulatory guidelines in all clinical research initiatives. By leveraging its extensive resources and expertise, NYU Langone Health aims to contribute significantly to the advancement of medical knowledge and the enhancement of patient care.

Locations

New York, New York, United States

Patients applied

0 patients applied

Trial Officials

Prashiela Manga, MD

Principal Investigator

New York University Medical School

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials