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Establishing a Descriptive Cohort of Patients Cared for Operation on the Spine

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02886260
Acronym
KEOPS
Enrollment
193
Registered
2016-09-01
Start date
2012-08-21
Completion date
2021-12-31
Last updated
2026-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Quality of Life, Spinal Diseases, Spinal Injuries

Brief summary

This study aims to: 1. describe the monitoring of patients treated for spinal disorders. 2. create a comprehensive database of reliable and readily exploitable quickly to produce a library of cross publications between orthopedic surgery and neurosurgical services. This database will include clinical, functional , radiographic , educational, social and professional data. 3. obtain a cohort of patients in the comprehensive range of spinal pathologies. 4. standardize data collection in this cohort with similar national projects.

Interventions

None listed

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The patient must be given free and informed consent and signed the consent * The patient must be affiliated or beneficiary of a health insurance plan * The patient is available for a 24-month follow-up * The patient is at least 18 years old * The patient has a symptomatic spinal pathology requiring surgical or orthopedic treatment

Exclusion criteria

* The patient is under judicial protection, guardianship or curatorship * The patient refuses to sign the consent * It is not possible to give informed information to the patient * The patient does not fluently read French. * the patient is not available for a 24-month follow-ip

Design outcomes

Primary

MeasureTime frame
Quality of life measured by the Oswestry Disability Index score24 months after surgical intervention

Secondary

MeasureTime frame
Quality of life measured by the Oswestry Disability Index score6 weeks, 12 weeks, 6 months, 12 months, 36 months, 48 months after surgical intervention

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 18, 2026