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effect of hyalorunidase and steroid epidural injection in lumbar spinal stenosis treatment

Not Applicable
Conditions
umbosacral spinal stenosis.
Spinal stenosis, lumbar region
M48.06
Registration Number
IRCT20171106037267N2
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Patients with lumbosacral spinal stenosis who have pain and other clinical symptoms didn’t respond to conservative management
Age between 45 to 75 y/o
Complete and sign constent form Exclusion

Exclusion Criteria

Diabetes mellitus
Rheumatologic disease such as collagen vascular disease , SLE , gout
Simultaneous radiculopathy
Simultaneous neuropathy
Brucella infection
BMI> 42
Knee arthroplasty in affected side
Coaglopathy
Inability to complete questionnaire and poor cooperation
Allergy to medication
Hepatic , renal or cardiac failure
Pregnancy
Cancer
Patients who are receiving Anticoagulant

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patient's pain. Timepoint: Before injection , 2, 4 and 8 weeks after injection. Method of measurement: Visual Analogue Scale , Quebec back pain disability scale and Oswestry disability index questionnaire.;Functional improvement. Timepoint: Before injection , 2, 4 and 8 weeks after injection. Method of measurement: Quebec back pain disability scale and Oswestry disability index questionnaire.
Secondary Outcome Measures
NameTimeMethod
?Quality of life improvement. Timepoint: Befor injection , 2, 4 and 8 weeks after injection. Method of measurement: Quebec back pain disability scale and Oswestry disability index questionnaire.;Decrease analgesic usage. Timepoint: Before injection , 2, 4 and 8 weeks after injection. Method of measurement: Visual Analogue Scale.
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