Clinical results of cement-augmented pedicle screw fixation in patients with osteoporosis

Not Applicable

Recruiting

• Conditions: Diseases of the musculoskeletal system and connective tissue

• Registration Number: KCT0005997
• Lead Sponsor: Yonsei University Health System, Severance Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 August 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

1)Patients over 20 years of age who are scheduled to perform posterior spinal instrumentation due to a thoracolumbar fracture or degenerative disease.
2)Patients with osteoporosis (T score = -2.5) on the bone mineral density test.
3)Patients judged by a surgeon that cement augmentation is necessary to obtain sufficient fixation of pedicle screws during surgery.
4)Patients who voluntarily agree to participate in this clinical trial

Exclusion Criteria

1)Patients undergoing spinal surgery for infection or spinal cord tumor.
2)Patients who undergoing interbody fusion
3)Patients judged unsuitable for participation in clinical trials by investigators

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative complication;screw loosening;fusion rate

Secondary Outcome Measures

Name	Time	Method
Distribution pattern of bone cement;Oswestry Disability Index (ODI) score