- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04060160
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
Status
Recruiting
Conditions
Intervention / Treatment
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
- Name: Alexander A. Navarini, Prof. Dr. MD
- Phone Number: +41 61 265 25 25
- Email: alexander.navarini@usb.ch
Study Contact Backup
- Name: Simon Müller, Dr. med
- Phone Number: +41 61 265 25 25
- Email: simon.mueller@usb.ch
Study Locations
-
-
-
Basel, Switzerland, 4031
- Recruiting
- Department of Dermatology, University Hospital Basel
-
Contact:
- Alexander A. Navarini, Prof. Dr. MD
- Phone Number: +41 61 265 25 25
- Email: alexander.navarini@usb.ch
-
Contact:
- Simon Müller, Dr. med
- Phone Number: 0041 61 328 6964
- Email: simon.mueller@usb.ch
-
Principal Investigator:
- Alexander Navarini, Prof. Dr. MD
-
Sub-Investigator:
- Dennis Arnold, Pract.med
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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
Additional Relevant MeSH Terms
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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