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Comparison of the effects of intra-articular injection of three drug combinations of high dose methylprednisolone and low dose methylprednisolone along with ketorolac and high dose ketorolac in knee osteoarthritis on reducing pain and increasing knee range of motion

Comparing the analgesic effects of intra-articular injection, high-dose methylprednisolone or low-dose methylprednisolone together with ketorolac or high-dose ketorolac in knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130304012695N20
Enrollment
75
Registered
2024-09-05
Start date
2024-10-06
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Osteoarthritis of knee. Osteoarthritis, unspecified site

Interventions

Intervention 1: Intervention group: Methylprednisolone group: methylprednisolone acetate, dose 80 mg, 2 mL, is injected with a 22 G needle in the flat knee and supine position and with the Midpatella

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Diagnosis of knee osteoarthritis based on ACR (American College of Rheumatology) criteria Failure to respond to drug and non-drug treatments during the last three months Articular cartilage destruction with grade 2 and 3 according to Lawrence-Kellgren criteria in radiological examination BMI less than 35 Patients aged 45-75 years

Exclusion criteria

Exclusion criteria: History of any joint injection or surgery on the knee Skin psoriasis at the injection site or septic arthritis Suffering from systemic diseases such as rheumatoid arthritis and diabetes, history of allergies and sensitivity to the drugs used The patient's unwillingness to participate in the study

Design outcomes

Primary

MeasureTime frame
Reducing knee pain and swelling. Timepoint: In the period of 2, 4, 8, 12 and 16 weeks after injection. Method of measurement: Numerical rating scale.;Increase the range of movement. Timepoint: In the period of 2, 4, 8, 12 and 16 weeks after injection. Method of measurement: Measuring the amount of increase in the leg movement angle around the knee joint.;Reducing the amount of systemic and analgesic drugs. Timepoint: In the period of 2, 4, 8, 12 and 16 weeks after injection. Method of measurement: Comparison of drug intake with before injection.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarsad Imani

Tehran University of Medical Sciences

imanifar@tums.ac.ir+98 21 6312 0000

Outcome results

None listed

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