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NCT07232238

TRPM2 Gene Polymorphism, NLRP3 Inflammasome Expression in Vitiligo Patients

Active, enrolled Last updated 31 December 2025
What this trial tests

trial in Vitiligo in 60 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
20 October 2025
Primary endpoint
1 October 2026
1 May 2027

Quick facts

Lead sponsorAswan University
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment60
Start date20 October 2025
Primary completion1 October 2026
Estimated completion1 May 2027
Sites1 location across Egypt

Conditions studied

Sponsor

Aswan University

Who can join

18 and older, any sex, with Vitiligo. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study investigates the relationship between Transient Receptor Potential Melastatin 2 (TRPM2) gene polymorphism and Nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3) inflammasome expression in patients with vitiligo. Vitiligo is a common autoimmune depigmenting disorder characterized by melanocyte destruction associated with oxidative stress and immune dysregulation. TRPM2 is a calcium-permeable cation channel activated by oxidative stress, while NLRP3 inflammasome activation promotes inflammation through interleukin-1β (IL-1β) and interleukin-18 (IL-18) release. This study aims to evaluate TRPM2 genetic variants, NLRP3 expression levels, and their possible correlation with disease severity measured using the Vitiligo Area Scoring Index (VASI).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Vitiligo

Currently open trials in the same condition.

Other Aswan University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07232238.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing