Comparison of transpedicular fixation with fusion with transpedicular fixation alone in spondylolisthesis: A Randomized Control Trial
Not Applicable
- Conditions
- Spondylolisthesis.SpondylolisthesisM43.1
- Registration Number
- IRCT20230907059376N3
- Lead Sponsor
- Afridi Medical Complex, Peshawar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 28
Inclusion Criteria
First and second grade degenerative lumbar spondylolisthesis patients
Patients who would consent to participating in the study under ethical conditions
Both Gender Male and Female
Age 18-45 years
Exclusion Criteria
Patients with additional lumbar spondylolisthesis types
Patients with additional lumbar degenerative spondylolisthesis grades (3rd and 4th grades)
Patients with additional spine pathology (lumbar fracture, disc prolapse)
Patients who respond to conservative treatment
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umbar spine disability. Timepoint: Post-surgery for baseline and then after 6 and 12 months. Method of measurement: Oswestry Disability Index (ODI).;Pain. Timepoint: Post-surgery for baseline and then after 6 and 12 months. Method of measurement: Visual analogue scale (VAS).
- Secondary Outcome Measures
Name Time Method