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The effect of Hyaluronidaz and Ozon on spinal canal stenosis

Comparing the effectiveness of intramuscular paravertebral injection of Oxygen –Ozone and epidural injection of Hyaluronidase on pain and function in patient with lumbosacral canal stenosis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191004044980N1
Enrollment
30
Registered
2019-11-25
Start date
2019-10-23
Completion date
Unknown
Last updated
2019-12-17

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: Injection of 18 cc Ozone-Oxygen mixture (2% _98%) at a concentration of 20 µg / dl at six points (three cc in each point) in the paravertebral muscles at 2 cm from

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: Back pain and other symptoms of spinal canal stenosis in the last six months Age between 35_75 years Confirmation of spinal canal stenosis through MRI and EDX

Exclusion criteria

Exclusion criteria: Diabetes Melitus Rheumatologic and collagen vascular diseases peripheral neuropathy and nerve injury Brucellosis BMI more than 41 History of trauma and spinal fracture Bleeding disorder Allergic reaction to Bovin protein Genetic disease such as Galactose intolerance or Lactase deficiency Patient with cardiac problem Inability to communicate and complete the questionnaire History of liver ,kidney and cardiopulmonary problem History of periarticular or intraarticular in the past 6 months Pregnant women People with cancer People taking Anticoagulant Favism

Design outcomes

Primary

MeasureTime frame
Pain score according to Visual Analog Scale. Timepoint: At baseline (before intervention), 2, 4 and 8 weeks after injection. Method of measurement: Visual Analog Scale.;Patient Performance Score in Oswestry Disability Scale. Timepoint: At baseline (before intervention), 2, 4 and 8 weeks after injection. Method of measurement: Oswestry Low Back Pain Questionnaire.;Patient Performance Score in QUEBEC Back Pain Disability. Timepoint: At baseline (before intervention), 2, 4 and 8 weeks after injection. Method of measurement: QUEBEC Back Pain Disability Qestionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReyhane Parvin

Shiraz University of Medical Sciences

Reyhaneh.parvin@gmail.com+98 71 5364 2641

Outcome results

None listed

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