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Cohort study of patients with thoracic spinal stenosis

Cohort study of patients with thoracic spinal stenosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102274
Enrollment
Unknown
Registered
2025-05-12
Start date
2023-07-30
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

thoracic spinal stenosis

Interventions

single thoracic ossification of ligamentum flavum without dural ossification for endoscopic surgery:None
Ossification of single thoracic ossification of ligamentum flavum without dural ossification for open surgery:None
Thoracic kyphosis Angle > 24.6°, or, fusion area kyphosis Angle > 23.0°:None
Thoracic kyphosis Angle <24.6°, or, fusion area kyphosis Angle <23.0°:None
other thoracic spinal stenosis patients:None

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1 Patients with thoracic spinal stenosis 2 over 18 years old 3 Patients with thoracic myelopathy or pain that was not relieved by conservative treatment were diagnosed with thoracic spinal stenosis by physical examination and imaging 4 Patients voluntarily participate in clinical research, sign informed consent, and can cooperate with clinical follow-up\

Exclusion criteria

Exclusion criteria: 1 Have participated in clinical trials of other drugs or hospital medical devices within the last 6 months 2 rheumatoid arthritis 3 Ankylosing Spondylitis 4 Diffuse Idiopathic Skeletal Hyperostosis 5 Combined with kidney, thyroid, parathyroid disease and other related diseases affecting endocrine or bone metabolism 6 A history of drug use that may affect bone calcium metabolism 7 Pregnant women or women planning to become pregnant and breastfeeding women 8 A person with mental disorder and no ability to act autonomously 9 Other conditions that the doctor judged could not be included in the experiment 10 Patients with MRI contraindications 11 Patients with systemic conditions that cannot tolerate surgery

Design outcomes

Primary

MeasureTime frame
Postoperative dysfunction;Perioperative complications;

Secondary

MeasureTime frame
Postoperative health recovery;

Countries

China

Contacts

Public ContactSun Chuguo

Peking University Third Hospital

sunchuiguo@163.com+86 139 1100 5426

Outcome results

None listed

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