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:
2025-12-24 @ 9:59 PM
Ignite Modification Date:
2025-12-24 @ 9:59 PM
NCT ID:
NCT04067232
Eligibility Criteria:
Inclusion Criteria:
* Patients with a one-sided posttraumatic impairment of forearm pro- and/or supination at least 3 months after injury
* Patients are above 18 years
* Patients who are willing to give informed consent
* National health insurance cover
Exclusion Criteria:
* A history of trauma to both forearms
* Any shoulder pathology or impairment preventing forward elevation of the arm as required during the scanning protocol
* Neuromuscular pathology
* Not able to understand or give informed consent
* Pregnancy (βHCG positive), breast-feeding or the absence of effective contraception for women of child-bearing age
* Legal incapacity (persons in custody or under guardianship)
* Deprived of liberty Subject (by judicial or administrative decision)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04067232
Study Brief:
Protocol Section:
NCT04067232