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Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis

NCT05145725 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 866

Last updated 2024-02-29

No results posted yet for this study

Summary

The study population concerns adolescent patients with idiopathic scoliosis which requires surgical management and who have a longer waiting period of 6 months.

The aim of this study is to research the predictive factors of an improvement in the quality of life of adolescents who have had surgery.

Conditions

  • Scoliosis; Adolescence
  • Arthrodesis

Interventions

BEHAVIORAL

Quality of life questionnaires

Different questionnaires to fill : SRS-22r, SF-36 score, TAPS, KIDSCREEN10

Sponsors & Collaborators

  • European Clinical Trial Experts Network

    collaborator OTHER

  • Asociación European Spine Study Group

    collaborator UNKNOWN

  • Elsan

    lead OTHER

Eligibility

Min Age
12 Years
Max Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-18
Primary Completion
2028-03-18
Completion
2036-03-18

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05145725 on ClinicalTrials.gov