Suspended

RAACAssesment of Enhanced Recovery After Pediatric Idiopathic Scoliosis Surgery

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Collected from past medical records and data - Retrospective
Who is being recruted

Bone Diseases+2

+ Musculoskeletal Diseases

+ Scoliosis

Until 18 Years
+4 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other

Utilizing specific methods not covered by standard models in order to address unique research questions.
Observational
Study Start: January 2018
See protocol details

Summary

Principal SponsorUniversity Hospital, Montpellier
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 1, 2018

Actual date on which the first participant was enrolled.

Enhanced recovery after surgery (ERAS) is a multimodal approach focused on reducing the stress response and associated physiologic changes related to surgery. Over the past 20 years, ERAS programs have been found to result in reduced lenght of stay and complications in adult patients. Data in pediatric population remains very scarce.Therefore this study was designed to compare the outcomes after scoliosis surgery before and after ERAS (enhanced recovery after surgery) program inplementation in children and teenager.

Official TitleAssesment of Enhanced Recovery After Pediatric Idiopathic Scoliosis Surgery
NCT04012528
Principal SponsorUniversity Hospital, Montpellier
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

150 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other

Some studies use unique or mixed approaches that don't fit standard categories. These may include innovative observational methods or studies tailored to specific research questions.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Until 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Bone DiseasesMusculoskeletal DiseasesScoliosisSpinal CurvaturesSpinal Diseases

Criteria

2 inclusion criteria required to participate
patient with age < 18 years

patient scheduled for scoliosis surgery

2 exclusion criteria prevent from participating
patient with age > 18years

patient with medical follow up by pediatric chronic pain departement

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Uh Montpellier

Montpellier, FranceOpen Uh Montpellier in Google Maps
SuspendedOne Study Center
RAAC | Assesment of Enhanced Recovery After Pediatric Idiopathic Scoliosis Surgery | PatLynk