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Imaging analysis, intraoperative evaluation, and postoperative evaluation of exacerbation of scoliosis

Imaging analysis, intraoperative evaluation, and postoperative evaluation of exacerbation of scoliosis - Imaging analysis, intraoperative evaluation, and postoperative evaluation of exacerbation of scoliosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000051812
Enrollment
300
Registered
2023-08-10
Start date
2017-01-27
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

scoliosis

Interventions

None listed

Sponsors

Toyama Univ
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who have scoliosis, are planning to undergo brace treatment or surgical treatment, and have given consent to participate in the study

Exclusion criteria

Exclusion criteria: 1. Preschool children under the age of 6 2. Patients who have difficulty filling out questionnaires or understanding tests due to dementia or intellectual disability 3. In the case of minors, patients without parental consent An orthopedic specialist determines the disease

Design outcomes

Primary

MeasureTime frame
Patient standing type QOL evaluation (ODQ, RDQ), Japanese scoliosis society evaluation sheet (SRS-22), spine simple CT, intraoperative cone-beam CT (before screw insertion, before and after correction), intraoperative dissection using Ponte device Evaluation of operation, evaluation of spinal cord blood flow, evaluation of spinal cord function monitoring, examination of bone metabolic dynamics (NTx, PTH, TRAP-5b), bone density, pre- and postoperative whole spine plain radiographs (standing front and lateral)

Countries

Japan

Contacts

Public ContactShoji Seki

Toyama Univ orthopedics

seki@med.u-toyama.ac.jp0764347353

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026