An observational study in Quality of Life, Spinal Injuries and Spinal Diseases, sponsored by Centre Hospitalier Universitaire de Nīmes. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-17.
Sponsored by Centre Hospitalier Universitaire de Nīmes · Observational
This study aims to:
57 studies on the registry are indexed under Spinal Injuries; 15 are open to participants now.
This study's enrollment of 193 is above the median of 92 across 22 observational studies indexed under Spinal Injuries.
Browse Spinal Injuries studies →Centre Hospitalier Universitaire de Nīmes is the lead sponsor of 595 studies on the registry; 90 are open to participants now.
Counted across the registry records on this site, refreshed daily.
patients with symptomatic spinal pathology requiring surgical or orthopedic treatment
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Quality of life measured by the Oswestry Disability Index score
Time frame: 24 months after surgical intervention
Quality of life measured by the Oswestry Disability Index score
Time frame: 6 weeks, 12 weeks, 6 months, 12 months, 36 months, 48 months after surgical intervention
Ran from Aug 2012 to primary completion in Dec 2021, 112 months.
How these figures are worked out, and which studies are left out of them.
This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.
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