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Classifications for Congenital Scoliosis

Reliability and Prognosis of Various Classifications for Congenital Scoliosis - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/01/100861
Enrollment
20
Registered
2026-01-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Q675- Congenital deformity of spine

Interventions

Intervention1: Nil: Nil

Sponsors

Kasturba Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children aged 0 to 18 years with a radiologically confirmed diagnosis of congenital scoliosis. Availability of adequate radiological imaging, including at least Standing full-length AP and lateral spine X-rays 3D CT scans (mandatory for prospective cohort; if available for retrospective cases) MRI spine to evaluate for intraspinal anomalies Ultrasound abdomen and echocardiography for evaluation of visceral anomalies Complete clinical records available for retrospective cases (demographics, imaging, follow-up). For the prospective cohort: Informed consent obtained from parents or legal guardians for participation and radiological evaluation.

Exclusion criteria

Exclusion criteria: Children with scoliosis of non-congenital etiology, including: Idiopathic scoliosis Neuromuscular scoliosis Syndromic scoliosis (e.g., Marfan, Ehlers-Danlos, Neurofibromatosis) Patients with inadequate or missing imaging or clinical documentation. Patients lost to follow-up Patients who have undergone prior spine surgery before initial radiological classification

Design outcomes

Primary

MeasureTime frame
Inter-rater Reliability of Congenital Scoliosis Classification SystemsTimepoint: At initial radiological evaluation using available imaging (X-ray CT MRI) Same time point for all three rater

Secondary

MeasureTime frame
Prognostic Value of Classification SystemsTimepoint: Baseline 6 months 12 months End of follow-up (maximum available duration)

Countries

India

Contacts

Public ContactDr. Hitesh Shah

Kasturba Medical College ,Manipal , Udupi

hitesh.Shah@manipal.edu9036251570

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026