Evaluation of Pain Following Scoliosis Surgery.

Evaluation of Pain Following Scoliosis Surgery.- RACHIDOL

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03686371

Acronym

RACHIDOL

Enrollment

Registered

2018-09-26

Start date

2018-01-02

Completion date

2019-06-30

Last updated

2023-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Scoliosis

Brief summary

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

Interventions

PROCEDUREposterior surgery for spinal arthrodesis

posterior surgery for spinal arthrodesis

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

10 Years to 18 Years

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

Design outcomes

Primary

Measure	Time frame	Description
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

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026