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Improved Rehabilitation After Spinal Surgery in Adolescents

CompletedNCT04183049
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Impact of the OFA technique on postoperative recovery from adolescent spine surgery and the incidence of chronic postoperative pain.

Study details

Official title
Improved Rehabilitation After Spinal Surgery in Adolescents: Prospective Observational Epidemiological Study of a Protocol Without Opioid
Conditions
Sponsor
Nantes University Hospital
Start date
2019-12-18
Primary completion
2021-08-01
Sex
All
Results posted
No results posted in this snapshot
Countries
France
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patent with idiopathic or secondary surgical scoliosis * Management by the paediatric anaesthesia team at the Mother and Child - Hospital of the University Hospital of Nantes * Non-opposition to inclusion in the study collected orally from the patient and parents * Satisfying oral and written comprehension of the French language, without interpreter * Ability to participate in a telephone interview Exclusion Criteria: * Patient that does not understand French correctly * Patient unable to express himself/herself correctly in French * Patient with a non-scoliotic surgical spinal pathology * Refusal to participate in the study * Absence of a record of non-opposition to participation in the study from the patient and his or her parents * Cerebral palsy or any other condition that does not allow participation in a telephone interview without particular difficulty.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04183049