RecruitingNCT05145725
Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis
Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis: Observational Study
Sponsor
Elsan
Enrollment
866 participants
Start Date
Mar 18, 2021
Study Type
OBSERVATIONAL
Conditions
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.
Eligibility
Min Age: 12 YearsMax Age: 20 Years
Inclusion Criteria4
- Patient between 12 and 20 years old
- Scoliosis in adolescents for whom surgery has been proposed based on radiological criteria (Cobb angle\> 25 ° for thoracolumbar and lumbar scoliosis,\> 35 ° for thoracic scoliosis and\> 40 ° for double major scoliosis)
- Patient affiliated or beneficiary of a social security scheme or attached to a beneficiary of a social security scheme
- Patient and legal representative having been informed and not opposing this research
Exclusion Criteria3
- Patient over 20 years old
- Non-surgical scoliosis
- Refusal to participate in the study by the child or parents
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Interventions
BEHAVIORALQuality of life questionnaires
Different questionnaires to fill : SRS-22r, SF-36 score, TAPS, KIDSCREEN10
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05145725
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