Comparison of oral pantoprazole and famotidine effect on new bone formation in patients with lumbar spine fusion surgery
Phase 3
Recruiting
- Conditions
- spondylosis.???? ? ???? ??? ???? ??(??????????)
- Registration Number
- IRCT20140915019185N4
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 58
Inclusion Criteria
patients with degenerative disease requiring lumbar fusion surgery for spinal canal stenosis .
patients with degenerative disease requiring lumbar fusion surgery for spondylolisthesis.
patients with degenerative disease requiring lumbar fusion surgery for deformity.
patients with degenerative disease requiring lumbar fusion surgery including discopathies .
Exclusion Criteria
Patients with low back injury due to trauma, infection, tumor, and inflammatory diseases, including rheumatoid arthritis
Patients with diabetes
Patients who smoke heavily
A person's BMI is less than 20 or more than 35
Patients who do not have the consent to enter the study
Patients with a history of osteoporosis are treated
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bone fusion. Timepoint: Before, three and six months after surgery. Method of measurement: Radiology and CT scan.
- Secondary Outcome Measures
Name Time Method