Minimally Invasive Surgery vs Standard Posterior Approach in the Treatment of Developmental Idiopathic Scoliosis
Recruiting now · Not applicable
Conditions studied: Adolescent Idiopathic Scoliosis
In brief
This is a randomized trial with 1:1 allocation. The aim of the study is to evaluate clinical and radiographic outcomes in patients with developmental age idiopathic scoliosis treated with mini invasive scoliosis surgery (MIS) technique versus posterior spinal fusion (PSF) technique through clinical and radiographic evaluations.
Key facts
- Study ID
- NCT05860673
- Run by
- Istituto Ortopedico Rizzoli
- People needed
- 126
- Starts
- 2023-07-15
- Expected to finish
- 2032-06-01
- Last updated by the study team
- 2025-06-04
Who can join
Age: 12 and older, up to 25. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with AIS
- Age between 12 and 25 years;
- Site of scoliotic curve: thoracic and/or lumbar;
- Preoperative radiographic range of the main scoliotic curve between 40° and 70° according to Cobb;
- Ability and consent of patients/parents to actively participate in the study and clinical follow-up.
You may not qualify if…
- Patients already treated surgically for scoliosis;
- Site of the scoliotic curve: cervical;
- Patients with scoliosis other than adolescent idiopathic scoliosis;
- Patients who do not fall within the described parameters;
- Unbalanced sagittal profile;
- Patients unable to consent or perform follow-ups.
- Pregnant women.
Where it is running
- Istituto Ortopedico Rizzoli — Bologna, Italy (enrolling)
Full record on ClinicalTrials.gov
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