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The effect of periarticular dextrose prolotherapy and ozone on knee osteoarthritis

The effect of combination of periarticular dextrose prolotherapy and ozone, on pain reduction in patients suffering from knee osteoarthritis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190415043279N8
Enrollment
28
Registered
2020-12-11
Start date
2020-03-20
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

knee arthritis. Bilateral primary osteoarthritis of knee

Interventions

Intervention 1: Intervention group: Injection into one of the joints, The amount of injection is 8 ml of 5% dextrose and 2 ml of 1% lidocaine and 5 ml of ozone. Three injections are given at weekly in

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with grade 2 and 3 osteoarthritis of both knees Age over 50 years Morning stiffness less than 30 minutes Crepitus in active knee movements Bone sensitivity Bone enlargement Lack of heat in the joint touch

Exclusion criteria

Exclusion criteria: Injection of steroid drugs in the last 2 months Diabetes Indication for surgical arthroplasty Previous injection treatment with dextrose Knee infection in the last three months Knee inflammation Daily use of drugs History of inflammatory joint disease Arthritis after infection Joint dysplasia Congenital anomalies Crystalopathy Arthritis after injury Malignancy Vascular necrosis Obesity Grade 4 osteoarthritis

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: Before intervention, one month after intervention, two months after intervention. Method of measurement: Visual Analogue Scale (VAS).;Physical function. Timepoint: Before intervention, one month after intervention, two months after intervention. Method of measurement: WOMAC Index.;Kellgrn lawrence index. Timepoint: Before intervention, one month after intervention, two months after intervention. Method of measurement: Radiological imaging.

Secondary

MeasureTime frame
Possible side effects. Timepoint: During the treatment period until the end of the intervention. Method of measurement: Any possible side effects such as pain, swelling, itching, redness and warmth at the injection site are measured and recorded.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Nasrin Moghimi

Sanandaj University of Medical Sciences

Nasrin_43ir@yahoo.com+98 87 3366 4645

Outcome results

None listed

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