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The clinical research of vertebral body stents

The clinical research of vertebral body stents

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIC-16008922
Enrollment
Unknown
Registered
2016-07-27
Start date
2013-10-16
Completion date
Unknown
Last updated
2017-04-18

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

experimental group:put a vertebral body into Vertebral body

Sponsors

Beijng Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. osteoporotic vertebral compression fractures; 3. sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. With a heart, cerebrovascular diseases; 2. Diseases of the blood clotting system; 3. Lactation or gestation or have a pregnancy plan within a month; 4. The vertebral canal with a larger bony and require surgical decompression; 5. Cleavage fracture; 6. Complete burst fracture; 7. The horizontal double column fracture; 8. Focused on dish of transverse ligament rupture of posterior fracture; 9. Mental illness; 10. Don't want to limit activities and don't follow the doctor's advice; 11. There are other surgical contraindications; 12. Participate in other clinical subjects in 3 months; 13. Researchers think the patients should not be included.

Design outcomes

Primary

MeasureTime frame
vision analogue score;vertebral body height;

Countries

China

Contacts

Public ContactTang Hai

Department of orthopedics, Beijng Friendship Hospital

tanghai@medmail.com.cn+86 13601362187

Outcome results

None listed

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