Surgical Outcome by Scrophy Pedicle in Spondylolisthesis Patients with and Without Modified Changes

Not Applicable

Recruiting

• Conditions: Spondylolisthesis patients.; Spondylolisthesis; M43.1

• Registration Number: IRCT20120527009878N10
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 October 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

All patients who have a back pain and will be screened for spondylolisthesis.

Exclusion Criteria

Patient dissatisfaction

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain in patients with and without changes in the mood. Timepoint: 6 to 12 months after surgery. Method of measurement: In follow-up, the pain of postoperative patients will be measured by strip tapeworm. The displacement and fracture of the screw will be evaluated by the postoperative control graph and the presence of infection or its absence with serial examinations will be evaluated every three to six months.