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 @ 9:31 PM
Ignite Modification Date:
2025-12-24 @ 9:31 PM
NCT ID:
NCT07140432
Eligibility Criteria:
Inclusion Criteria:
* Patients over 21 years of age
* Patients who have undergone cervical arthrodesis and are being treated at Clinique de la Sauvegarde or Clinique Convert
* Patients with a NDI clinical score at 1 year greater than 5
* Patient affiliated to/ or beneficiary of a Social Security scheme as definied by the law
Exclusion Criteria:
* Patients whose clinical condition requires rapid treatment that can't wait for examinations to be carried out
* Pregnancy and breastfeeding
* Protected person (curatorship, guardianship, safeguard of justice)
* History of hypersensitivity to the active substance ( sodium oxidronate) or to any of its constituents
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
21 Years
Maximum Age:
99 Years
Study:
NCT07140432
Study Brief:
Protocol Section:
NCT07140432