Comparison of the effects of Alendronate and Vitamin D administration on lumbosacral vertebral fusio

Phase 3

• Conditions: spinal fusion.; Osseous stenosis of neural canal; M99.3

• Registration Number: IRCT20180826040869N2
• Lead Sponsor: Mazandaran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 18 May 2020

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 75

Inclusion Criteria

Lumbar discopathy patients
spinal canal stenosis
lumbar Listis
Cr <1.2
age between 20 and 65 years

Exclusion Criteria

Patients with traumatic lesions
Neoplastic lesions
Infectious lesions
Surgical history
Disabling underlying problems and rheumatic diseases
Patients with a history of osteoarthritis and vitamin D deficiency less than 10 units
Patients with renal insufficiency and GFR below 40

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Percentage of people with no fusion. Timepoint: Patients will be re-examined and fusion of the vertebrae one month, three months, and six months after surgery. Method of measurement: Check CT scan stereotype.;Percentage of people with low pain scores. Timepoint: Patients will be re-examined for pain severity one month, three months, and six months after surgery. Method of measurement: From the visual analog scale vas (visual Analog Scale).