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The effect of ozone-oxygen gas on pain and activity in patients with lumbar spinal stenosis

Not Applicable
Conditions
lumbar spinal stenosis.
Spinal stenosis, lumbar region
M48.06
Registration Number
IRCT20190419043319N1
Lead Sponsor
Yazd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
84
Inclusion Criteria

Informed consent to participate in the study
Existence of neurological pain and lameness in the last six months
Age between 35-75 years
Absence of any spinal or musculoskeletal disease
No response to drug treatment for more than 3 months

Exclusion Criteria

Diabetes mellitus
Body mass index more than 41
History of fracture of the spine
History of bleeding disorders
Rheumatic diseases
Neuropathy
Psychological diseases
Brucellosis
Genetic diseases such as galactose intolerance or lactase deficiency
Congenital heart diseases
Allergic reactions to bovine proteins
Inability to communicate
History of significant liver, kidney and heart disorders
Injections in or around the affected joint in the last six months
Pregnancy
Cancer
People who are taking anticoagulants
People with Favism
Vascular claudication
History of previous spinal surgery
Indication of emergency surgery
Any ban on ozone treatment
Any ban on acetaminophen
People consuming codeine

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before treatment, immediately after treatment, and at weeks 4 and 8 after treatment. Method of measurement: Somatic symptom scale questionnaire.;Physical activity. Timepoint: Before treatment, immediately after treatment, and at weeks 4 and 8 after treatment. Method of measurement: Somatic symptom scale questionnaire.;Satisfaction. Timepoint: Before treatment, immediately after treatment, and at weeks 4 and 8 after treatment. Method of measurement: Somatic symptom scale questionnaire.
Secondary Outcome Measures
NameTimeMethod
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