Evaluation of Pain Following Scoliosis Surgery.

NCT03686371 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 51

Last updated 2023-04-13

No results posted yet for this study

Summary

The main objective of this study was to evaluate acute pain following scoliosis surgery in adolescent.

Conditions

  • Idiopathic Scoliosis

Interventions

PROCEDURE

posterior surgery for spinal arthrodesis

posterior surgery for spinal arthrodesis

Sponsors & Collaborators

  • Rennes University Hospital

    lead OTHER

Principal Investigators

  • Anne DEFONTAINE, MD · Rennes University Hospital

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-02
Primary Completion
2018-10-23
Completion
2019-06-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03686371 on ClinicalTrials.gov