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ERAS and Pediatric Scoliosis Surgery

NCT ID: NCT04012528

Last Updated: 2020-12-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-01-01

Study Completion Date

2021-11-30

Brief Summary

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The aim of this study is to compare the outcomes after scoliosis surgery before and after ERAS (enhanced recovery after surgery) program inplementation in children and teenager.

Detailed Description

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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.

Conditions

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Scoliosis

Keywords

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Pediatric Surgery Rehabilitation

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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"the before" group

75 teenagers after scoliosis surgery before ERAS program implementation

ERAS program

Intervention Type OTHER

ERAS program

"the after" group

75 teenagers after scoliosis surgery after ERAS program implementation

No interventions assigned to this group

Interventions

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ERAS program

ERAS program

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patient with age \< 18 years
* patient scheduled for scoliosis surgery

Exclusion Criteria

* patient with age \> 18years
* patient with medical follow up by pediatric chronic pain departement
Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Montpellier

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Chrystelle CS SOLA, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Montpellier

Locations

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Uh Montpellier

Montpellier, , France

Site Status

Countries

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France

Other Identifiers

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RECHMPL18_0382

Identifier Type: -

Identifier Source: org_study_id