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Observation on the Clinical Efficacy of Percutaneous Curved Vertebral Pseudo-implantation in Osteoporotic Vertebral Compression Fractures

Observation on the Clinical Efficacy of Percutaneous Curved Vertebral Pseudo-implantation in Osteoporotic Vertebral Compression Fractures

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129463
Enrollment
Unknown
Registered
2026-08-05
Start date
2026-03-10
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Osteoporotic Vertebral Compression Fractures

Interventions

Percutaneous Curved Vertebroplasty group:None
Percutaneous Vertebroplasty group:None

Sponsors

Yantaishan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Diagnosed with vertebral compression fractures by MRI; 2. Age >= 60 years; 3. Single-segment vertebral fracture; 4. T value detected by dual-energy X-ray densitometry is less than -2.5, indicating osteoporosis; 5. Complete imaging data; 6. No symptoms of spinal cord or nerve root compression; 7. The patient or legal representative has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Accompanied by blood coagulation disorders; 2. Accompanied by tumor or infection; 3. Poor cardiopulmonary function or combined with other diseases that cannot tolerate surgery; 4. Incomplete imaging data and follow-up records.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale score;Oswestry Disability Index score;The anterior height of the vertebral body (AVH);Bone cement distribution;

Secondary

MeasureTime frame
Cobb angle;Middle height of the vertebral body (MVH);Surgical complications;

Countries

China

Contacts

Public ContactDu Wei

Yantaishan Hospital

duwdoc@163.com+86 535 686 3895

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026