Skip to main content
OpenTrials
Completed

NCT Number: NCT02886260

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Quality of Life Back Injuries Bone Diseases Musculoskeletal Diseases Spinal Diseases Spinal Injuries Wounds and Injuries

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU Nimes

Nîmes, 30000, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Quality of life measured by the Oswestry Disability Index score

    Time frame: 24 months after surgical intervention

Secondary outcomes

  1. 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

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nīmes

Other

Registry information

Acronym: KEOPS

Important dates

Study start
2012
Primary completion
2021
Study completion
2021
First posted
Sep 1, 2016
Registry last updated
Jun 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.