Evaluation of Pain Following Scoliosis Surgery.

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

Completed

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Key information

Conditions

Idiopathic Scoliosis

Age range

10 year–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU de Rennes

Rennes, 35033, France

Who can participate

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

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

Treatment and study plan

posterior surgery for spinal arthrodesis

Procedure

posterior surgery for spinal arthrodesis

Primary outcomes

Visual Analog Score for pain (EVA)

Time frame: 3 days after inclusion

The assessment criteria used is the numerical pain scale from 0 to 10(0 = no pain, 10 = extremely painful

Sponsors and collaborators

Lead sponsor

Rennes University Hospital

Other

Registry information

Official study title

Evaluation of Pain Following Scoliosis Surgery.- RACHIDOL

Acronym: RACHIDOL

Important dates

Study start: 2018
Primary completion: 2018
Study completion: 2019
First posted: Sep 26, 2018
Registry last updated: Apr 13, 2023

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.

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

Completed