Actively Recruiting

Phase Not Applicable
Age: 12Years - 25Years
All Genders
NCT05860673

Minimally Invasive Surgery vs Standard Posterior Approach in the Treatment of Developmental Idiopathic Scoliosis

Led by Istituto Ortopedico Rizzoli · Updated on 2025-06-04

126

Participants Needed

1

Research Sites

463 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Minimally Invasive Surgery vs Standard Posterior Approach in the Treatment of Developmental Idiopathic Scoliosis

Who Can Participate

Age: 12Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with adolescent idiopathic scoliosis
  • Age between 12 and 25 years
  • Scoliotic curve located in the thoracic and/or lumbar region
  • Main scoliotic curve with a Cobb angle between 40° and 70° before surgery
  • Ability and consent to actively participate in the study and attend clinical follow-ups
Not Eligible

You will not qualify if you...

  • Previous scoliosis surgery
  • Scoliotic curve located in the cervical spine
  • Scoliosis types other than adolescent idiopathic scoliosis
  • Patients outside the defined curve or age parameters
  • Unbalanced sagittal spinal profile
  • Unable to consent or participate in follow-ups
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Istituto Ortopedico Rizzoli

Bologna, Italy, 40136

Actively Recruiting

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Research Team

A

Alessandro Gasbarrini, MD

CONTACT

B

Bruna Maccaferri, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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