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Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis (APOSIA)

E

Elsan

Status

Enrolling

Conditions

Arthrodesis
Scoliosis; Adolescence

Treatments

Behavioral: Quality of life questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT05145725
2020-A03069-30

Details and patient eligibility

About

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.

Enrollment

866 estimated patients

Sex

All

Ages

12 to 20 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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 criteria

  • Patient over 20 years old
  • Non-surgical scoliosis
  • Refusal to participate in the study by the child or parents

Trial design

866 participants in 1 patient group

Idiopathic scoliosis in adolescents requiring surgery
Treatment:
Behavioral: Quality of life questionnaires

Trial contacts and locations

1

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Central trial contact

Jean-François Oudet

Data sourced from clinicaltrials.gov

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