Acne Detection Software (AcneDect) (AcneDect)

April 11, 2022 updated by: University Hospital, Basel, Switzerland

Acne Detection Software (AcneDect); AcneDect: a Software to Detect Acne Lesions

This study is to create a self-learning software that can detect acne lesions. Patients take a picture of their face every single day for 3 months with a secure mobile phone and fill out a pre-designed questionnaire. After 3 months, the mobile will be collected back and the pictures will be evaluated by 3 dermatologists. The software is able to learn from the dermatologists' evaluation and -using machine learning- a mechanism that should be able to automatically detect acne to some extent will be established.

Study Overview

Study Type

Observational

Enrollment (Anticipated)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Basel, Switzerland, 4031
        • Recruiting
        • Department of Dermatology, University Hospital Basel
        • Contact:
        • Contact:
        • Principal Investigator:
          • Alexander Navarini, Prof. Dr. MD
        • Sub-Investigator:
          • Dennis Arnold, Pract.med
        • Sub-Investigator:
          • Simon Müller, Dr. med

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

10 years to 35 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients within the consultation service of Dermatologische Klinik, Universitätsspital Basel, that meet the inclusion criteria

Description

Inclusion Criteria:

  • Acne vulgaris

Exclusion Criteria:

  • Refusal to participate

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pictures to train the AcneDect software
Time Frame: every single day from baseline for 3 months
Collection of pictures to train the AcneDect software to detect change in acne lesions
every single day from baseline for 3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
AcneDect questionnaire regarding acne burden (Visual Analogue Scale (VAS) scale ranging from "Not bad at all" to "Very bad")
Time Frame: every single day from baseline for 3 months
Collection of patient reported outcomes via a mobile electronic case report form
every single day from baseline for 3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Alexander A. Navarini, Prof. Dr. MD, Dermatologische Klinik; Universitätshospital Basel

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 29, 2020

Primary Completion (Anticipated)

December 1, 2022

Study Completion (Anticipated)

December 1, 2022

Study Registration Dates

First Submitted

August 15, 2019

First Submitted That Met QC Criteria

August 15, 2019

First Posted (Actual)

August 16, 2019

Study Record Updates

Last Update Posted (Actual)

April 12, 2022

Last Update Submitted That Met QC Criteria

April 11, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 2018-00702; sp19Navarini

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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