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Trial · NCT07907744

Plasma Exeresis Plus NB-UVB Versus NB-UVB Alone for Stable Vitiligo

NCT07907744, Not applicable, Active not recruiting, University of Faisalabad

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Plasma Exeresis Plus NB-UVB Versus NB-UVB Alone for Stable Vitiligo. Trials, record NCT07907744. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07907744

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Plasma Exeresis Plus NB-UVB Versus NB-UVB Alone for Stable Vitiligo
NCT number
NCT07907744
Status
Active not recruiting
Phases
Not applicable
Enrollment
70 participants, actual
Lead sponsor
University of Faisalabad
Conditions
Vitiligo
Interventions
Plasma Exeresis, Narrowband Ultraviolet B (NB-UVB) Phototherapy
First posted
2026-10-30
Last updated
2026-11-03

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in Vitiligo Area Scoring Index (VASI) from Baseline to Week 24Baseline to Week 24
Treatment efficacy will be assessed by measuring the change in the Vitiligo Area Scoring Index (VASI) from baseline to Week 24. The VASI is a validated clinical scoring system used to assess the extent of vitiligo and the degree of depigmentation. The score is based on the percentage of body surface area affected by vitiligo and the degree of depigmentation within the affected areas. Higher VASI scores indicate greater disease severity, whereas lower scores indicate less extensive vitiligo and improvement. The VASI score has a theoretical minimum of 0, indicating no vitiligo, and a maximum of 100, representing complete depigmentation of the entire body surface area. A reduction in VASI score from baseline to Week 24 indicates improvement in vitiligo severity. A reduction of 50% or more from baseline will be considered a clinically significant improvement.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07907744

GET https://conductscience.org/api/trials/v1/NCT07907744/registered