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OpenTrials
Completed

NCT Number: NCT06213545

Diagnostic Accuracy of Teledermatology in Patch Test Interpretation

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of medicine, Siriraj hospital, Mahidol university

Bangkoknoi, Bangkok, 10700, Thailand

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

In-clinic interpretation

Diagnostic Test

Reading patch test result at clinic

Photo interpretation

Diagnostic Test

Reading patch test result by sending photo to clinic

Primary outcomes

  1. grading of patch test

    Time frame: 48 hours, 72 hours and 7 days

    sucess, intermediate and failure

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Acronym: Tele patch

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jan 19, 2024
Registry last updated
Nov 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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