Development of Automated Real-time Algorithms for Detection of Dislocation of the Carpus (CARPUS)

November 7, 2023 updated by: University Hospital, Strasbourg, France

Study CARPUS : " Development of Automated Real-time Algorithms for Detection of Dislocation of the Carpus "

Perilunate dislocation of the carpus is a serious lesion of the wrist which is defined by a total loss of contact of the articular surfaces capito-lunar, scapholunate and lunate-triquetral. Rare by its frequency, it represents 5 to 10% of traumatic injuries of the wrist.

Perilunate wrist dislocation is a rare injury that goes unnoticed in 25% of cases. Even with surgical treatment, 50-100% of patients will develop radiocarpal and/or midcarpal osteoarthritis.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

10100

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

  • France
      • Strasbourg, France, 67091
        • Recruiting
        • Service de Chirurgie de la main - CHU de Strasbourg - France
        • Contact:
        • Principal Investigator:
          • Philippe LIVERNEAUX, MD, PhD
        • Sub-Investigator:
          • Sybille FACCA, MD, PhD
        • Sub-Investigator:
          • Marie-Cécile SAPA, MD
        • Sub-Investigator:
          • Kévin Delplanque, Statistician
        • Sub-Investigator:
          • Maxence Gabet, Statistician
        • Sub-Investigator:
          • Sébastien Pouilly, Statistician
        • Sub-Investigator:
          • Pierre Debruyne, Statistician
        • Contact:

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Major subjects (≥18 years old) treated at the University Hospitals of Strasbourg for a carpal dislocation between 01/01/2012 and 31/12/2022.

Description

Inclusion criteria :

  • Major subjects (≥18 years old)
  • Treated at the University Hospitals of Strasbourg for a carpal dislocation
  • Presence of carpal radiographs that may indicate the presence of a lesion
  • Subjects who have not expressed their opposition, after information, to the re-use of their data for the purposes of this research

Exclusion criteria :

  • Subject having expressed his opposition to participate in the study
  • Subject under legal protection, guardianship or curatorship

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
Time Frame
Retrospective analysis of carpal X-rays for the development of an algorithm to automatically identify the presence of pathology in the carpal anatomical area
Time Frame: Files analysed retrospectively from January 01, 2012 to December 31, 2022 will be examined]
Files analysed retrospectively from January 01, 2012 to December 31, 2022 will be examined]

Collaborators and Investigators

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

Sponsor

University Hospital, Strasbourg, France

Investigators

  • Principal Investigator: Philippe LIVERNEAUX, MD, PhD, Service de Chirurgie de la main - CHU de Strasbourg - France

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)

June 1, 2022

Primary Completion (Estimated)

December 1, 2023

Study Completion (Estimated)

December 31, 2023

Study Registration Dates

First Submitted

July 8, 2022

First Submitted That Met QC Criteria

July 13, 2022

First Posted (Actual)

July 14, 2022

Study Record Updates

Last Update Posted (Estimated)

November 8, 2023

Last Update Submitted That Met QC Criteria

November 7, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 8559 (FDA)

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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