Results of L4-L5-S1 vertebral fusion treatment with L5-S1 in patients with L5-S1 spondylolisthesis
Not Applicable
- Conditions
- Spondylolisthesis.M43.1Spondylolisthesis
- Registration Number
- IRCT20201130049541N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
High grade L5-S1 spondylolisthesis
Candidate for vertebral fusion operation with instrumentation
Slip on the surface of a Vertebrae
Patient consent to participate in the study
Age less than 60 years
Exclusion Criteria
Patients with neurological defects and in need of emergency surgery
Patients with a history of underlying diabetes and neuropathy
Patients with a history of heart disease and preoperative anticoagulant use
Patients who smoke and are addicted to drugs and alcohol
Patients with metabolic bone diseases
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain. Timepoint: Before, one month, three months and six months after surgery. Method of measurement: Using the visual pain scale (VAS).
- Secondary Outcome Measures
Name Time Method