Skip to content

Study of the Efficacy of Ozone Injection on low back pain

A Comparative Study of the Efficacy of Ozone Injection with Two Doses and Oxygen Injection on Pain and Physical Function of Patients with Radicular Low back pain: A Controlled Randomized Trial with A six-Month Follow –up

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211116053072N1
Enrollment
54
Registered
2023-05-31
Start date
2023-06-05
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Condition 1: Radicular Low Back Pain. Condition 2: DISC HERNIATION. Low back pain Unspecified thoracic, thoracolumbar and lumbosacral intervertebral disc disorder

Interventions

Intervention 1: Intervention group: Patients receiving a dose of 40 micrograms per milliliter of ozone or group O3 40mg. Intervention 2: Intervention group: Patients receiving a dose of 20 micrograms

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with diffuse low back pain with minimal pain intensity 4 according to VAS criteria At least 1 month of low back pain Failure to respond to supportive therapy (such as medication or physiotherapy) Age 30-60 years old Patients with body mass index 20-35 MRI based on the presence of a disc herniation whose location is associated with symptoms

Exclusion criteria

Exclusion criteria: Previous spinal surgery Bone lesions of the spine or spinal cord History of receiving ozone or topical injection of any other drug Pregnancy Spinal cord diseases Uncontrolled diabetes

Design outcomes

Primary

MeasureTime frame
Patient with low back pain on minimum scale 4 of VAS. Timepoint: before the study, 3 month and 6 month after the beginning. Method of measurement: VAS questionnaire.;Functional progress in patient with low back pain. Timepoint: before the study, 3 month and 6 month after the beginning. Method of measurement: functional tests.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Urumieh

Iran University of Medical Sciences

marziehorumieh@gmail.com+98 21 6655 4259

Outcome results

None listed

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