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Preliminary study of minimally invasive spine surgery guided by ultrasound combined with C-arm

Preliminary study of minimally invasive spine surgery guided by ultrasound combined with C-arm

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080422
Enrollment
Unknown
Registered
2024-01-29
Start date
2023-04-04
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Osteoporotic compression fractures

Interventions

Percutaneous kyphoplasty ultrasound group:The puncture was performed under ultrasound guidance
Normal group of percutaneous kyphoplasty:No intervention
Percutaneous vertebroplasty ultrasound group:The puncture was performed under ultrasound guidance
Normal group of percutaneous vertebroplasty:No intervention
Transforaminal endoscopic puncture and ultrasound-guided observation group:The puncture was performed under ultrasound guidance
The control group was guided by transforaminal endoscopic puncture and ultrasound:No intervention

Sponsors

The Second Affiliated Hospital of Hunan University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria of PKP group: (1) age 55-85 years old; (2) T value of bone mineral density < -2.5 SD. (3) any single vertebral compression fracture of T10-L5 confirmed by imaging. (4) Non-other pathological fractures. (5) The injured lumbar spine had obvious kyphosis. (6) can tolerate surgical treatment and cooperate with follow-up. A total of 40 patients were enrolled and randomly divided into ultrasound group and C-arm X-ray group, with 20 patients in each group. PVP group inclusion criteria: (1) age 55-85 years old; (2) T value of bone mineral density < -2.5 SD. (3) any single vertebral compression fracture of T10-L5 confirmed by imaging. (4) Non-other pathological fractures. (5) can tolerate surgical treatment and cooperate with follow-up. A total of 40 patients were enrolled and randomly divided into ultrasound group and C-arm X-ray group, with 20 patients in each group. The inclusion criteria of the transforaminal endoscopic group were as follows: age 55-85 years old; The patient had clinical symptoms of lumbar disc herniation and was diagnosed by imaging examination. Surgical treatment was needed if conservative treatment failed for 2 months. Single segment, unilateral lumbar disc herniation; Patients and their families were informed and agreed to participate in the study. A total of 40 patients were enrolled and randomly divided into ultrasound group and C-arm X-ray group, with 20 patients in each group.

Exclusion criteria

Exclusion criteria: Exclusion criteria of PKP group: (1) patients could not tolerate surgical treatment; (2) The fracture was burst fracture with occupying bone in the spinal canal or spinal cord nerve injury. (3) The fracture was pathological and the skin condition at the surgical site was poor. (4) PVP was selected when the injured vertebrae had obvious kyphosis. Exclusion criteria of PVP group: (1) unable to tolerate surgical treatment; (2) The fracture was burst fracture with occupying bone in the spinal canal or spinal cord nerve injury. (3) The fracture was pathological and the skin condition at the surgical site was poor. Exclusion criteria of the transforaminal endoscopic group: previous history of surgery that caused spinal structure defects; Combined with multi-segmental disc herniation; Lumbar segmental instability; Combined with lumbar spinal stenosis; There were surgical contraindications.

Design outcomes

Secondary

MeasureTime frame
Visual analogue scale;Oswestry disability index;Japanese Orthopaedic Association Scores;

Primary

MeasureTime frame
Time of puncture;Bone cement perfusion volume;Duration of local anesthesia;Pedicle positioning time;Total operative time;Intraoperative fluoroscopy times;

Countries

China

Contacts

Public ContactJINGQI ZENG

The Second Affiliated Hospital of Hunan University of Traditional Chinese Medicine

3238216159@qq.com+86 139 7313 7130

Outcome results

None listed

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