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Effect of Transpedicular Prying Reduction Following Distraction with Monoaxial Screws in Short Same-Segment Fixation via the Wiltse Approach on Thoracolumbar Burst Fractures Without Neurologic Deficit

Effect of Transpedicular Prying Reduction Following Distraction with Monoaxial Screws in Short Same-Segment Fixation via the Wiltse Approach on Thoracolumbar Burst Fractures Without Neurologic Deficit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108971
Enrollment
Unknown
Registered
2025-09-09
Start date
2025-09-12
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

single-segment unstable thoracolumbar burst fracture

Interventions

transpedicular pry reduction (TPR) technique following distraction:transpedicular pry reduction (TPR) technique following distraction
traditional distraction-only reduction:traditional distraction-only reduction

Sponsors

The First People's Hospital of Bengbu City
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age range: 18-60 years old, gender is not limited. 2. Fresh burst fracture of single segment thoracolumbar spine (T11-L2) (injury to surgery time 1/3, or kyphotic Cobb Angle>15 °, or spinal canal invasion>30% (measured by CT). 4. No neurological damage (ASIA grade E). 5. Sign a written informed consent form, voluntarily participate and be able to complete the follow-up.

Exclusion criteria

Exclusion criteria: 1. Combined spinal cord or nerve root injury (ASIA grades A-D). 2. Multi segmental spinal fractures or severe injuries in other areas require priority treatment. 3. Pathological fractures (tumors, infections, etc.). 4. Severe osteoporosis (dual energy X-ray absorptiometry bone density T value <= -3.0). 5. Have a history of spinal surgery at the same level in the past. 6. Unable to tolerate general anesthesia or posterior surgery. 7. Surgical contraindications include severe heart, lung, liver, kidney dysfunction, coagulation dysfunction, etc. 8. Unable to cooperate with research and follow-up due to mental illness or cognitive impairment. 9. Pregnant or lactating women. 10. Other situations that researchers consider unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Recovery rate of anterior vertebral body height after surgery (%);

Secondary

MeasureTime frame
Radiological indicators;Clinical Outcomes: VAS score;Safety Indicators;

Countries

China

Contacts

Public ContactSheng Shi

The First People's Hospital of Bengbu City

shisheng273@163.com+86 137 6172 9084

Outcome results

None listed

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