Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:16 AM
Ignite Modification Date:
2025-12-25 @ 2:16 AM
NCT ID:
NCT03308760
Eligibility Criteria:
Inclusion Criteria:
* persons informed about the research
* sportsmen and women (competition or leisure, practiced \> 3h/week)
* Between 18 and 45 years old
* First episode of acute traumatic unilateral rupture of the Achilles tendon
* Open surgery in the Orthopaedic and Traumatology Department of Dijon University Hospital
* Identical post-operative immobilisation programme for 6 weeks
* Absence of major post-operative complications delaying the rehabilitation
Exclusion Criteria:
* persons without national health insurance cover
* concomitant joint disease that could be aggravated by the tests
* heart disease/contra-indication to effort required during the isokinetic test
* management other than open surgery (orthopaedic, functional, percutaneous surgery, …)
* Rupture of the contralateral tendon
* Contra-indication for the use of the Biodex S4 pro
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT03308760
Study Brief:
Protocol Section:
NCT03308760