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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05575596
Other study ID # ISASE001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 14, 2022
Est. completion date November 2024

Study information

Verified date March 2023
Source University Hospital, Caen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The incidence of idiopathic scoliosis is 3% or approximatively 300,000 new cases per year in France. It is estimated that between 0.1 and 0.3% of patients will eventually require surgical management, between 500 and 1000 scoliosis are operated per year in France. To our knowledge, the impact of socio-economic and territorial inequalities on the quality of life before and after surgery of idiopathic scoliosis has not been studied previously. Main objective: -Assess the impact of socio-economic and territorial inequalities on the pre- and post-operative quality of life at 1 year after surgical idiopathic scoliosis management, in a French pediatric surgery multicenter cohort. Secondary objective: - Assess the impact of socio-economic and territorial inequalities on the quality of life pre and postoperative at 3 months after surgery on a French multicenter cohort. - To assess the impact of severity and type of scoliosis on pre- and post-operative quality of life at 3 months and 1 year after surgery on a French multicenter cohort.


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date November 2024
Est. primary completion date November 2024
Accepts healthy volunteers
Gender All
Age group 10 Years to 25 Years
Eligibility Inclusion Criteria: - Operated by posterior vertebral arthrodesis - Opereted in pediatric surgery center - Idiopathic scoliosis treated by surgery Exclusion Criteria: - Refusal to participate - People unable to read or speak French (the questionnaire being in French) - Non-idiopathic scoliosis

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France DOLET Nathan Caen Calvados

Sponsors (6)

Lead Sponsor Collaborator
University Hospital, Caen Amiens University Hospital, Hôpital Necker-Enfants Malades, Hopital Universitaire Robert-Debre, University Hospital, Lille, University Hospital, Rouen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline quality of life (SRS-22) at one year after surgery depending on the socio-economic level and remoteness. We will use the SRS-22 questionnaire, a specific questionnaire validated in French to assess the quality of life of patients with scoliosis.
The questionnaire coverts different part of socio-economic levels including the salary, the educational level, the type of social security coverage, the parents' family situation (single parent, two-parent, blended couple) and the number of people and pieces in the habitation.
The remoteness will be evaluated by the distance between the medical referent center and the habitation.
At 1 years after surgery. Baseline questionnaire will be assessed just before the surgery
Secondary Radiological data: angulation parameters Scoliosis radiological parameters before and after surgery (just after and at 1 year after surgery) cobb, kyphosis, lordosis, pelvic incidence (unit of measure: angulation in degrees) at the time of surgery and at one year fater surgery
Secondary Radiological data : type of scoliosis Scoliosis radiological parameters before and after surgery (just after and at 1 year after surgery): type of scoliosis (lenkee classification) at the time of surgery and at one year fater surgery
Secondary Clinical data: age Age at diagnosis and at surgery in months at the surgery
Secondary Clinical data: weight weight (in kilograms) at the surgery
Secondary Clinical data: previous treatments previous treatment for scoliosis (yes or no) at the surgery
Secondary Clinical data: family history history of scoliosis in the family (yes or no) at the surgery
Secondary Surgery data Type of instrumentation, level of instrumentation, surgical complications (neurological, infectious). during the firts year after the surgery
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