Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age12-20
SponsorElsan
About this trial
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 criteria
Qualifiers
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
Disqualifiers
Patient over 20 years old
Non-surgical scoliosis
Refusal to participate in the study by the child or parents
Trial design
Treatments tested in this trial
- Quality of life questionnaires
Treatment groups
866 Participants
are divided into 1 treatment groupSponsors and collaborators
Elsan
Lead sponsor
European Clinical Trial Experts Network
Collaborator
Asociación European Spine Study Group
Collaborator
Source ClinicalTrials.gov