NCT07055009

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
47

participants targeted

Target at P25-P50 for all trials

Timeline
8mo left

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress63%
Mar 2025Dec 2026

Study Start

First participant enrolled

March 30, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

June 4, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 8, 2025

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2026

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

July 8, 2025

Status Verified

May 1, 2025

Enrollment Period

1.2 years

First QC Date

June 4, 2025

Last Update Submit

July 3, 2025

Conditions

Keywords

Actinic prurigosubtype actinic prurigoHLA typinggenetic

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

Diagnostic Test: Targeted long-read HLA sequencingOther: RNA extractionOther: Full Skin examination

Control

Diagnostic Test: Targeted long-read HLA sequencingOther: RNA extraction

Interventions

Genetic study

Also known as: Short-read whole genome sequencing
CaseControl

Nanostring technology, Seattle

CaseControl

Skin and mucosa examination

Case

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

Actinic Prurigo

Central Study Contacts

Einapak Boontaveeyuwat, MD

CONTACT

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

Locations