ClinicalTrials.Veeva

Menu

Self-perceived Health Status and Healthcare Consumption of Idiopathic Scoliosis Patients Treated More Than 20 Years Ago: How Much do Operated and Non-operated Patients Differ? (HISTORY)

U

University Hospital, Strasbourg, France

Status

Enrolling

Conditions

Adolescent Idiopathic Scoliosis

Treatments

Other: Group comparaison

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Adolescent idiopathic scoliosis (AIS) is a common condition that affects millions of patients worldwide. This is characterized by a spinal deformity that leads to a deformation of the trunk, an imbalance of the shoulders and waist folds as well as the appearance of gibbosity.

Posterior arthrodesis correction is a common practice surgery for the treatment of AIS after failure of medical treatment with a corset or functional rehabilitation. Surgery allows functional improvement and is indicated for curves greater than medically treated scoliosis.

The objective of this international study is to have a better understanding of the long-term outcomes (> 20 years of follow-up) after treatment (surgical and non-surgical) of AIS and to compare the long-term status of the patient with AIS to the general population of the same age, sex and comorbidities.

All of this information will help justify or modify the strategy, techniques and goals of early treatment in adolescence to achieve a better long-term outcome.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of Adolescent Idiopathic Scoliosis
  • Main baseline curve magnitude over 40º
  • Aged 10 to 18 years at the time of treatment (surgical or nonsurgical)
  • More than 20 years of follow up
  • Current contact information available

Exclusion criteria

  • Non-idiopathic scoliosis
  • Younger than 10 or older than 18 at the time of initial treatment
  • Less than 20 years of follow up
  • Patients unable to understand and answer the questionnaires because of language difficulties or because of cognitive impairments

Trial design

100 participants in 2 patient groups

Non-Surgical Group
Description:
Patients treated non-surgically during adolescence (\<18 years of age) with a baseline Cobb \>40º and minimum 20 years of follow-up.
Treatment:
Other: Group comparaison
Surgical Group
Description:
Patients treated surgically during adolescence (\<18 years of age) with a baseline Cobb \>40º, and minimum 20 years of follow-up
Treatment:
Other: Group comparaison

Trial contacts and locations

2

Loading...

Central trial contact

Yann Philippe CHARLES

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems