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Comparison of the effect of 2% Atorvastatin gel on clinical symptoms of knee osteoarthritis

A comparative evaluation of the effect of 2% Atorvastatin gel versus Diclofenac gel on clinical symptoms of patients with knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150706023084N6
Enrollment
40
Registered
2020-08-17
Start date
2017-12-20
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

Knee Osteoarthritis.

Interventions

Intervention 1: Intervention group: Atorvastatin Gel prepared by researcher, Knee local use, 2 times a day for 3 months. Intervention 2: Control group: diclofenac gel 1 % (Razak) ,2 times daily, for

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Diagnosis of mild to moderate knee osteoarthritis by a rheumatologist based on cilinical symptoms and knee X-ray No other topical treatments usage at least tow weeks before the study No oral Atorvastatin usage No other systemic analgesics or anti-inflammatory usage at least tow weeks before the study Obtaining informed consent from the patients patients aged between 40 and 75 years old

Exclusion criteria

Exclusion criteria: Those who need to use other oral or intravenous analgesics Unwilling to continue or to participate in the study any further Patients with other knee joint disorders: ( Rhumatoid Arthrities, Gout, Pseudo Gout, Infected Arthrities ) Knee corticosteroid injection in the past 3 months Joint replacement Pregnancy and lactation Sensitivity to study drugs

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: At the beginning of the study,4weeks,8weeks,12weeks after treatment. Method of measurement: WOMAC Questionnaire.;Stiffness. Timepoint: At the beginning of the study,4weeks,8weeks,12weeks after treatment. Method of measurement: WOMAC Questionnaire.;Physical Function. Timepoint: At the beginning of the study,4weeks,8weeks,12weeks after treatment. Method of measurement: WOMAC Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNiloofar Sadat Mousanejad

Islamic Azad University

niloofar_mousanejad@yahoo.com+98 21 2284 3946

Outcome results

None listed

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