Percutaneous Stabilization of thoracolumbal spine fractures

Recruiting

• Conditions: spine fracture; S32; Fracture of lumbar spine and pelvis

• Registration Number: DRKS00005052
• Lead Sponsor: niversitätsklinikum Düsseldorf, Klinik für Unfall- und Handchirurgie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-09-23
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 125

Inclusion Criteria

a. Acute (< 3 weeks) traumatic injuries from T1 to L5 with percutaneous internal fixation

b.written consent

Exclusion Criteria

a. concomitant injuries, which influence spine function
b. pediatric fractures c. kyphoplasty d.no written consent

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Spine function (VAS Spine Score) after implant removal (9-12 months postoperative)

Secondary Outcome Measures

Name	Time	Method
radiographic evaluation of the segmental kyphosis and the wedging deformity of the involved vertebral body performed during clinical follow up