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A Predictive Model for Assessing Prognosis in Adolescent Scoliosis Correction Surgery Based on Preoperative CT Imaging Parameters—A Retrospective Clinical Study

A Predictive Model for Assessing Prognosis in Adolescent Scoliosis Correction Surgery Based on Preoperative CT Imaging Parameters—A Retrospective Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114727
Enrollment
Unknown
Registered
2025-12-17
Start date
2025-12-19
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Scoliosis

Interventions

Group of Patients Undergoing Adolescent Scoliosis Correction:None

Sponsors

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 17 Years

Inclusion criteria

Inclusion criteria: 1.Conformed to the diagnostic criteria for adolescent idiopathic scoliosis (AIS). 2.Aged from 10 to 17 years, inclusive. 3.Rated as ASA physical status I to III. 4.Scheduled for elective posterior approach spinal deformity correction and fusion surgery under general anesthesia at Nanjing Drum Tower Hospital between June 2018 and April 2025. 5.Possession of measurable non-contrast CT imaging data acquired within 1 month prior to the surgery.

Exclusion criteria

Exclusion criteria: 1. Non-idiopathic scoliosis (e.g., congenital, neuromuscular, syndromic scoliosis); 2. History of previous spinal surgery; 3. Patients with severe comorbidities involving cardiac, cerebral, hepatic, or renal dysfunction; 4. Accompanied by severe neuromuscular diseases, connective tissue disorders, or skeletal dysplasia syndromes; 5. Underwent anterior approach surgery or revision surgery for scoliosis; 6. Incomplete key clinical data.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative hypotension;

Secondary

MeasureTime frame
Blood loss;Duration of intraoperative hypotension (defined as MAP 65 mm Hg is sustained for 20 s);Types and total dosage of rescue vasopressor agents administered during the perioperative period;Duration of use and postoperative complications within 3 days (e.g., pneumothorax, hypoxemia, heart failure, infection, incidence of postoperative AKI);

Countries

china

Contacts

Public ContactSun Yu'e

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School

13913846977@126.com+86 139 1384 6977

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026