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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06213545
Other study ID # COA 589/2566(IRB3)
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date September 18, 2023
Est. completion date September 30, 2024

Study information

Verified date January 2024
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to learn about accuracy of teledermatology in patch test interpretation in patch test's patients population. The main question[s] it aims to answer are: - Accuracy of teledermatology in patch test interpretation by dermatologist - Accuracy of teledermatology in patch test interpretation by Residency - Accuracy of teledermatology in patch test interpretation by Scitentist - The factors influencing the interpretation of remote dermatologic patch test results from photographs of patients. Participants will - do patch test in Siriraj hospital and come to follow up at 48 hr and 72 hr for interpretation of patch test - take a photo at home and sent the photo to contact clinic via online application or email on the day of 48 hr, 72 hr and 7 days following the interpretation of patch test Researchers will compare in-clinic group and telephoto group to see if the accuracy of patch test interpretation is more or less.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 108
Est. completion date September 30, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Participants in the study must be 18 years of age or older. - Participants in the study must have undergone patch testing for contact allergies. - Participants in the study should be able to take photos of test results on their back and/or arms using a mobile phone or personal camera, and send them to the researcher through the Line application and/or email within 48 hours, 96 hours, and on the 7th day. - Participants in the study should be able to read and comprehend the questionnaire in Thai and respond to the questionnaire independently. - Participants in the study must have at least one positive result in the patch testing. - Participants in the study must provide consent to participate in the study by signing the informed consent document. Exclusion Criteria: - Participants in the study who are unable to attend follow-up appointments for result assessments.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
In-clinic interpretation
Reading patch test result at clinic
Photo interpretation
Reading patch test result by sending photo to clinic

Locations

Country Name City State
Thailand Faculty of medicine, Siriraj hospital, Mahidol university Bangkoknoi Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary grading of patch test sucess, intermediate and failure 48 hours, 72 hours and 7 days
See also
  Status Clinical Trial Phase
Completed NCT05625295 - Tele-dermatology Non-presential (TeleDermaSA)
Completed NCT00013234 - Health Services Implications of a Teledermatology Consult System N/A