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 @ 11:19 PM
Ignite Modification Date:
2025-12-24 @ 11:19 PM
NCT ID:
NCT03832556
Eligibility Criteria:
Inclusion Criteria:
* Adult patient with neurogenic para-osteo-arthropathy resulted by prior central nervous system, cerebral or medullar damage
* Deformation with limitation of articular amplitude which could result limitation in rehabilitation care
* An indication of partial or total surgical excision of heterotopic ossification
* Indication of pre-operative assessment by CT scan and MRI, with contrast product injection
* Signed consent of patient obtained after clear and relevant informations given by physician
* Patient covered by social security
Exclusion Criteria:
* Contraindications to an MRI examination: cardiac stimulator, metallic intraocular foreign bodies...
* Contraindications to CT scan
* Contraindications to contrast injection product, such as iodinated or gadolinium-based contrast media
* Impractical venous access
* Severe deformation resulting impossibility to positioning for MRI examination or CT scan
* Patient can not give consent
* Participation to another interventional study
* Patient under guardianship
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03832556
Study Brief:
Protocol Section:
NCT03832556