Multi-centred Clinico-genetic Study of Actinic Prurigo in Thailand
1 other identifier
observational
47
1 country
1
Brief Summary
This research project investigates the clinical and genetic associations of Actinic Prurigo (AP) in the Thai population. As a rare chronic photodermatosis, AP has been observed to occur more frequently in individuals with certain genetic predispositions, particularly specific Human Leukocyte Antigen (HLA) types. Previous studies have suggested variations in clinical presentation and HLA allele distributions between Asian and Western populations. The primary aim is to explore the relationship between clinical manifestations of AP and genetic profiles, including HLA typing, among Thai individuals. Additionally, the study seeks to examine whether different HLA types are associated with varying responses to treatment. The study design is a cross-sectional comparative study, involving both AP patients and age-matched healthy controls. Given the rarity of the condition, patient recruitment will be conducted across four collaborating institutions: King Chulalongkorn Memorial Hospital Siriraj Hospital Institute of Dermatology
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Mar 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 30, 2025
CompletedFirst Submitted
Initial submission to the registry
June 4, 2025
CompletedFirst Posted
Study publicly available on registry
July 8, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
July 8, 2025
May 1, 2025
1.2 years
June 4, 2025
July 3, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Targeted long-read HLA sequencing
Correlation between the occurrence of Actinic Prurigo (AP), its clinical manifestations, and genetic factors-including HLA types-in individuals of Thai ancestry.
through study completion, an average of 1 year
Secondary Outcomes (2)
Short-read whole genome sequencing (WGS)
through study completion, an average of 1 year
Immunology study
through study completion, an average of 1 year
Study Arms (2)
Case
Control
Interventions
Genetic study
Eligibility Criteria
Actinic Prurigo (AP)
You may qualify if:
- Thai ethnicity
- Diagnosed with Actinic Prurigo (AP) according to the diagnostic criteria defined for this study
- Mentally competent, able to communicate, and able to read Thai.
- Participants receiving Thalidomide treatment must use two simultaneous methods of contraception, starting at least 4 weeks prior to initiating the medication and continuing throughout the treatment period and for at least 4 weeks after discontinuation.
You may not qualify if:
- History and physical examination findings suggestive of other photodermatoses such as Lupus erythematosus, Porphyria, or Polymorphous Light Eruption, among others.
- Elevated Epstein-Barr Virus (EBV) viral load detected in blood testing (EBV viral load will be tested in all participants).
- Low Minimal Erythema Dose (MED) to UVB radiation as the only abnormal finding.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Medicine Chulalongkorn University
Bangkok, Thailand
MeSH Terms
Conditions
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- OTHER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 4, 2025
First Posted
July 8, 2025
Study Start
March 30, 2025
Primary Completion (Estimated)
May 31, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
July 8, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will not share