The efficacy of vitamin D and oral alendronate on Modic change
Phase 2
Completed
- Conditions
- Condition 1: Lumbar discopathy. Condition 2: Spinal stenosis. Condition 3: Lumbar listesis.
- Registration Number
- IRCT20140915019185N2
- Lead Sponsor
- Sari University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
Female patients with lumbar degenerative diseases undergoing pedicular screw fusion up to 4 level
Exclusion Criteria
Patients with infection,tumor,diabetes,history of previous surgery, rheumatoid diseases
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Modic change. Timepoint: FIRS of study,6 month after study. Method of measurement: MRI.;Pain. Timepoint: 0,1,3,6. Method of measurement: Visual Analogue Scale.;Ability to do daily work. Timepoint: 0,1,3,6. Method of measurement: Oswestry Disability Index.
- Secondary Outcome Measures
Name Time Method