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Clinical study of unilateral angular kyphoplasty in the treatment of senile osteoporotic vertebral compression fracture

Clinical study of unilateral angular kyphoplasty in the treatment of senile osteoporotic vertebral compression fracture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107088
Enrollment
Unknown
Registered
2025-08-04
Start date
2024-02-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Osteoporotic vertebral compression fracture

Interventions

Experimental Group: Unilateral Oblique Puncture PCK:Surgical treatment of osteoporotic vertebral compression fracture by unilateral angular puncture percutaneous kyphosis
Control Group: Bilateral PKP:Bilateral percutaneous kyphosis for osteoporotic vertebral compression fractures

Sponsors

Nanan District People's Hospital of Chongqing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients of either gender, aged 60 years or older.2.A confirmed diagnosis of a single vertebral compression fracture, as evidenced by X-ray, CT, or MRI imaging.3.A BMD T-score of less than -2.5 SD, indicating the presence of osteoporosis.4.Absence of spinal cord or nerve compression symptoms.5.Time interval from onset of symptoms to surgery not exceeding one week.6.Provision of informed consent by the patient.

Exclusion criteria

Exclusion criteria: 1.Multiple vertebral fractures; 2.Combined with other parts of the fracture; 3. Malignant tumors or metastatic vertebral tumors; 4.severe coagulation dysfunction; 5.vertebral infectious diseases, systemic or local soft tissue infections; 6.accompanied by spinal cord compression or nerve injury and compression symptoms; 7.Severe spinal deformity, mental disease or other diseases, unable to cooperate with prone position during the operation; 8.Allergic to bone cement, unable to operate.

Design outcomes

Primary

MeasureTime frame
Surgical Time;Intraoperative Blood Loss;Intraoperative C-arm Fluoroscopy Usage;Intraoperative C-arm Fluoroscopy Usage;Bone Cement Distribution;Visual analogue scale;Oswestry disability index;Cobb Angle;

Countries

China

Contacts

Public ContactChuanjiang Xie

Nanan District People's Hospital of Chongqing

365524290@qq.com+86 189 8392 9427

Outcome results

None listed

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