Comparative study of lumbar spine stabilization with 2-stage surgery and cement augmentatio

Not Applicable

• Conditions: umbar spine degeneration.; Other degenerative diseases of the nervous system; G30-G32

• Registration Number: IRCT20230222057496N3
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

Osteoporosis patients with pre-surgery bone density in the range (T-Score->2.5)
age range over 50 years
body mass index between 20-30
with degenerative lumbar spine complications at L1-S1 level is

Exclusion Criteria

Patients who could not be reached or lived outside the province
pationts did not want to enter the study
The presence of other pathological factors (cysts or tumors)
discopathy in other vertebrae
performing any re-surgery during the past year
using narcotics or narcotic drugs and smoking
suffering from underlying diseases affecting Osteoporosis (rheumatoid arthritis, thyroid disorders...)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Before surgery - one month after surgery. Method of measurement: VAS visual analog scale.;Disability of patients. Timepoint: Before surgery - one month after surgery. Method of measurement: Oswestry Disability Index (ODI).

Secondary Outcome Measures

Name	Time	Method
Fution. Timepoint: 12 months after surgery. Method of measurement: BSF classification scale.;Pedicle Screw loosing. Timepoint: 12 months after surgery. Method of measurement: Dynamic radiography and CT scan images.