Dow International Medical College , DUHS, Karachi, Sindh, Pakistan - 01 Jan `25Efficacy and Safety of Apremilast in Combination with NBUVB and NBUVB Alone in Vitiligo Patients

Efficacy and Safety of Apremilast in Combination with NBUVB and NBUVB Alone in Vitiligo Patients

Official title: Comparison Between Apremilast in Combination with NBUVB and NBUVB Alone in Vitiligo - a Randomized Controlled Trial

Status: Enrolling by invitation

Description:

Patients of non-segmental vitiligo, fulfilling the inclusion criteria will be selected from the OPD, dermatology department. It's an interventional study where Group A patient will be given NBUVB and Tab Apremilast 30 mg twice a day and Group B will receive NBUVB alone.

Phase: Phase 4.

What is being studied: combination product — Apremilast with NB-UVB; device — NB-UVB.

Who can take part: ages 18 Years to 70 Years, 30 participants planned.

Enrollment status: Invitation only. The study started 01 January 2025 and is expected to finish 30 March 2027.

Source: ClinicalTrials.gov, NCT06593197 (https://clinicaltrials.gov/study/NCT06593197).

Start date: January 01, 2025

Completion date: March 30, 2027

Organizer: Dow University of Health Sciences

Link: https://clinicaltrials.gov/study/NCT06593197

The registry does not list a contact for this study. Use the link above to reach the study record on ClinicalTrials.gov.

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FAQOther Questions

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