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

evaluation of the efficacy of hyaluronidase and steroid epidural injection compared with hypertonic saline and steroid epidural injection in the treatment of lumbosacral spinal stenosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171106037267N2
Enrollment
30
Registered
2018-02-10
Start date
2017-12-22
Completion date
Unknown
Last updated
2018-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbosacral spinal stenosis. Spinal stenosis, lumbar region

Interventions

Intervention 1: Intervention group: will receive hyalorunidase 1500 IU , methylprednisolone 80 mg, and marcaine 4cc.the injection will be done under fluoroscopic guide and after contrast media inject

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
?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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alireza Ashraf

Shiraz University of Medical Sciences

an_ghorbani@sums.ac.ir+98 71 3231 9040

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026