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A clinical trial of percutaneous vertebroplasty with high viscosity bone cement

A clinical trial of percutaneous vertebroplasty with high viscosity bone cement

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004835
Enrollment
Unknown
Registered
2014-06-23
Start date
2015-01-01
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, vertebral hemangioma and spinal metastases

Interventions

Control group:Use of ordinary bone cement in vertebral plasty
Experimental group:Use of ordinary bone cement in vertebral plasty

Sponsors

Daping Hospital of the Third Affiliated Hospital of Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Osteoporosis: osteoporotic vertebral compression fractures, pain symptoms after conservative treatment are still unable to ease or to prevent complications of long-term bed cause; 2. Vertebral body of primary and metastatic malignant tumors: pain symptoms, after chemotherapy or radiotherapy can't ease; 3. Vertebral hemangioma; 4. Part of the vertebral body benign tumor

Exclusion criteria

Exclusion criteria: 1. Asymptomatic stable fractures; 2. Patients improved obviously after medical treatment; 3. No evidence of acute fractures patients preventive treatment; 4.Blood coagulation dysfunction or have a bleeding tendency; 5. The target is vertebral osteomyelitis; 6. Allergic to surgery need anything; 7. The root of pain and significantly more than the pain of vertebral body, caused by the compression syndrome of has nothing to do with the vertebral body collapse. 8. Cause obvious vertebral canal compression fracture displacement; 9. Vertebral compression degree of more than 75%; 9. Vertebral fracture over the trailing edge vertebral bodies or trailing edge fracture vertebral bodies;10.Unable tolerate surgery

Design outcomes

Primary

MeasureTime frame
Visual Analogue Score;Lumbar spine X-ray;Oswestry disability index;ncidence, predisposing factors of mesh-related com;

Countries

China

Contacts

Public ContactJianhua Zhao

Department of Spinal Surgery, Da Ping hospital, Third military medical university, Chongqing, China

medic_stu-wz@163.com+86 13330230836

Outcome results

None listed

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