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Effects of clacitonin epidural injection in patients with spinal canal stenosis

Phase 2
Recruiting
Conditions
degenerative spinal canal stenosis.
Spinal stenosis
Registration Number
IRCT20120814010599N24
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Unresponsive to usual low back pain treatments
American society of Anesthesiologists class 1,2

Exclusion Criteria

Diabetes
Anxiety or depression disorder
coagulopathy or bleeding tendency
addiction
drug allergy
local infection on the site of injection or systemic infection
Patient dissatisfaction
History of spinal surgery
traumatic causes
Congenital spinal cord defect
Progressive neurological defect

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain score and function before and after injection. Timepoint: before injection, 4, 8 and 12 weeks after. Method of measurement: OSWESTRY Disability Index ( ODI index ) and Numeric Rating scale ( NRS ).
Secondary Outcome Measures
NameTimeMethod
Evaluation the quality of life. Timepoint: Before injection, 4, 8 and 12 weeks later. Method of measurement: ODI index( OSWESTRY Disability Index).
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