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Clinical Trials/NCT07174024
NCT07174024CompletedPhase 4

A Comparative Study on the Efficacy of Blue Light Emitting Diodes Therapy Versus Targeted Narrow Band UVB in Stable Non-segmental Vitiligo Patients.

Cairo University1 site in 1 country30 target enrollmentStarted: January 20, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Assess the degree of improvement in vitiligo pigmentation using VASI scores before and after treatment.

Study Overview

Brief Summary

A comparative study on the efficacy of blue light emitting diodes therapy versus targeted Narrow band UVB in stable non-segmental vitiligo patients.

Detailed Description

A comparative study on the efficacy of blue light emitting diodes therapy versus targeted Narrow band UVB in stable non-segmental vitiligo patients.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •All age group.
  • •Both genders.
  • •Subjects with stable non-segmental vitiligo (≥2 patches) acral or non-acral patches of diameter ≤ 2cm.

Exclusion Criteria

  • •Prior treatment with laser therapies for at least 3 months
  • •Recent exfoliation procedures.
  • •Recent surgical procedures.
  • •Poor skin conditions including keloids.
  • •Hypersensitivity to light ( visible and near-infrared).
  • •Medications that make users more sensitive to light.
  • •Anticoagulant and immunosuppressive treatments.
  • •Gestations or breastfeeding.
  • •A personal or family history of skin cancer.
  • •Unstable vitiligo (older lesions have not progressed for the last 1 years and lack of Koebner phenomena ).

Arms & Interventions

patients will receive NB-UVB phototherapy sessions on a Randomly selected patch

Active Comparator

patients will receive NB-UVB phototherapy sessions on a Randomly selected patch

Intervention: Narrow Band UVB Treatment (Device)

Patients will receive blue light emitting diodes phototherapy on a randomly selected patch

Active Comparator

Patients will receive blue light emitting diodes phototherapy on a randomly selected patch

Intervention: blue light emitting diode (Device)

Outcomes

Primary Outcomes

Assess the degree of improvement in vitiligo pigmentation using VASI scores before and after treatment.

Time Frame: 48 weeks

Assess the degree of improvement in vitiligo pigmentation using VASI scores before and after treatment.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nahla Maher Mahmoud Mahran

Lecturer of Dermatology

Cairo University

Study Sites (1)

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