Evaluation of Pain Following Scoliosis Surgery.

Completed

• Conditions: Idiopathic Scoliosis

• Registration Number: NCT03686371
• Lead Sponsor: Rennes University Hospital

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2018-01-02
• Study First Submitted: 2018-09-10
• Study First Submitted QC: 2018-09-25
• Study First Posted: 2018-09-26
• Primary Completion: 2018-10-23
• Study Completion: 2019-06-30
• Status Verified: 2023-04
• Last Update Submitted: 2023-04-11
• Last Update Posted: 2023-04-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 51

Inclusion Criteria

• adolescent from 10 to 18 years of age
• idiopathic scoliosis
• posterior surgery for spinal arthrodesis
• non opposition children and parents

Exclusion Criteria

• complication following surgery needing reoperation
• secondary intervention
• anterior surgery
• non idiopathic scoliosis

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Visual Analog Score for pain (EVA)	3 days after inclusion	The assessment criteria used is the numerical pain scale from 0 to 10(0 = no pain, 10 = extremely painful

Trial Locations

Locations (1)

CHU de Rennes; 🇫🇷 Rennes, France