Stress Response Pathways in Vitiligo



Status:Recruiting
Conditions:Dermatology
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:18 - 50
Updated:11/18/2018
Start Date:October 2015
End Date:December 2022
Contact:Megan McLachlan
Email:mclacm01@nyumc.org

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Stress Response Pathways in Vitiligo: A Prospective, Investigator Initiated, Interventional Study With Two Arms

The purpose of this study is to investigate stress response pathways in tissues and
melanocytes from patients with vitiligo. Investigators are collecting evidence of UPR and
stress response activation in tissues and melanocytes from patients with vitiligo.
Individuals with vitiligo will have punch biopsies to study stress response UPR activation
and NF-κB signaling to test our hypothesis. In order to characterize differences between
disease and normal states, a second arm of control individuals (Arm 2) will be recruited.

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.

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
We found this trial at
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550 1st Ave
New York, New York 10016
(212) 263-7300
Principal Investigator: Prashiela Manga, MD
New York University School of Medicine NYU School of Medicine has a proud history that...
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