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Active, not recruitingNCT06370650Updated Apr 17, 2024

Effect of Platelet Rich Plasma on Outcome of Narrow Band UVB in Treatment of Vitiligo; Clinical and Histopathological Study

An interventional study of platelet rich plasma, narrow band UVB in Management of Stable Vitiligo, sponsored by Sohag University. Active, not recruiting at 1 site in Egypt. Open to participants aged 15 Years to 50 Years. Per ClinicalTrials.gov, last updated 2024-04-17.

Sponsored by Sohag University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Dec 2023, registered Apr 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
15 Years to 50 Years
Sex
All
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Study summary

For each patient, one side of body will be treated with NB-UVB alone while the other side will be treated with NB-UVB therapy in addition to intradermal injection of PRP every 2 weeks. Patients will be photographed at the first visit, in the middle and at the end of therapy. Each patient will sign a written consent form to be included in the study and to be photographed.

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Conditions studied

  • Management of Stable Vitiligo

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03

In context

Vitiligo

298 studies on the registry are indexed under Vitiligo; 69 are open to participants now.

This study's enrollment of 30 is close to the median of 30 across 227 interventional studies indexed under Vitiligo.

Browse Vitiligo studies →

Lead sponsor

Sohag University is the lead sponsor of 1,183 studies on the registry; 612 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
15 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Patients with stable non segmental vitiligo. (Absence of koebnerization, absence of new lesion and absence of widening of the existing lesions).

Patients have more than 15 years.

Exclusion criteria

-

Exclusion Criteria:

Patients have active vitiligo (appearance of new lesion, history of koebnerization).

Pregnant and lactating women. History of keloid formation. Anemia (hemoglobin level \<10gm/dl), thrombocytopenia (platelet count \<100,000 /µL), coagulopathies or patients on anticoagulant therapy and patients with iron deficiency.

Patients taking drugs that prolong bleeding time such as Aspirin and vitamin E Patients taking treatment of vitiligo in last 2 months

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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Active comparator
    Narrow band UVB

    Procedure: platelet rich plasma, narrow band UVB

  • Active comparator
    Platelet rich plasma plus narrow band UVB

    Procedure: platelet rich plasma, narrow band UVB

Interventions

  • Procedureplatelet rich plasma, narrow band UVB

    Role of PRP in treating stable vitiligo

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What researchers measure

Primary outcomes

  1. Improvement of vitiligo

    increase repigmentation score

    Time frame: within 6 months

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Study locations

1 site
  • Faculty of Medicine, Sohag University
    Sohag, 82515, Egypt
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References and documents

Individual participant data

Plan to share: Undecided — Researcher shall pubish in national journal

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 17, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06370650
Lead sponsor
Sohag University
Responsible party
Sara Hassan Ahmed (assissant lecturer, Sohag University) — Principal investigator
First posted
Apr 17, 2024
Start date
Dec 8, 2023
Primary completion
Jan 25, 2024
Completion
Jun 30, 2024 (estimated)
Last update
Apr 17, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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