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Active, not recruitingNCT07760441RespiScoUpdated Aug 12, 2026

Cardiorespiratory Assessment Prior to Scoliosis Surgery: a 10-year Experience at a Specialized Scoliosis Center

An observational study in Scoliosis, Restrictive Pulmonary Disease and Pulmonary Hypertension, sponsored by Poitiers University Hospital. Active, not recruiting at 1 site in France. Per ClinicalTrials.gov, last updated 2026-08-12.

Sponsored by Poitiers University Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
174
Sex
All
01

Study summary

this study involves adult patients who underwent scoliosis surgery within the last 10 years. The aim of this study is to assess the frequency of scoliosis-related respiratory complications in patients requiring orthopedic surgery, in order to optimize the care pathway for patients with scoliosis.

In this context, we use the medical data collected and generated during the treatment of scoliosis, as well as the results of tests and samples taken during your hospitalization to calculate the prevalence of respiratory and cardiac impairments associated with scoliosis

02

Conditions studied

  • Scoliosis
  • Restrictive Pulmonary Disease
  • Pulmonary Hypertension
  • Restrictive Breathing Pattern
03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients who underwent scoliosis surgery in the past 10 years in Poitiers hospital

Inclusion criteria

  • respiratory function test or echocardiography \<2ans

Exclusion criteria

Exclusion Criteria:

  • \<18 years old
04

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
174 participants (actual)
Patient registry
No

Interventions

  • Procedurerespiratory function test

    respiratory test and transthoracic ultrasound

05

What researchers measure

Primary outcomes

  1. restrctif pulmonary disorder prevalence

    Time frame: 2015 - 2025

06

Study locations

1 site
  • University Hospital Poitiers
    Poitiers, 86000, France
07

Registry details

Key details

Study ID
NCT07760441
Lead sponsor
Poitiers University Hospital
Responsible party
Sponsor
First posted
Aug 12, 2026
Start date
Apr 1, 2026
Primary completion
Apr 1, 2026
Completion
Jan 1, 2027 (estimated)
Last update
Aug 12, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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