MedPath

Effect of Zingiber zerumbet pomade in treatment of knee arthrosis

Phase 3
Recruiting
Conditions
Osteoarthritis.
Arthrosis, unspecified
Registration Number
IRCT20170428033670N1
Lead Sponsor
Immunology Research Center of Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

Out-patients who suffer osteoarthritis based on clinical criteria of ACR

Exclusion Criteria

Those who need more than 2 grams of acetaminophen daily
Those who need to use other oral or intravenous analgesic
Sensitivity to study drugs
Patients with Secondary osteoarthritis caused by rheumatic diseases such as rheumatoid arthritis
Pregnancy
Joint Replacement
Concomitant use of glucosamine and chondrotin sulfate
Knee corticosteroid injection in the past 3 months
Oral or topical use of Corticosteroid in 14 past days
Other Articular corticosteroid injection in the past 1 months
Mussle corticosteroid injection in the past 1months
Skin Diseases in Knee
Radiculopathy and Neuropathy
Alcohol addicted, Drug Abuse
Patients with active Renal, Liver, and Peptic Ulcer Diseases
Age under 30 or over 80 years

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before the intervention, the end of the second week and the end of the fourth week after the start of the intervention. Method of measurement: The Western Ontario and McMaster Universities Osteoarthritis (WOMAC) questionnaire.;Physical Function. Timepoint: Before the intervention, the end of the second week and the end of the fourth week after the start of the intervention. Method of measurement: The Western Ontario and McMaster Universities Osteoarthritis (WOMAC) questionnaire.;Stiffness. Timepoint: Before the intervention, the end of the second week and the end of the fourth week after the start of the intervention. Method of measurement: The Western Ontario and McMaster Universities Osteoarthritis (WOMAC) questionnaire.
Secondary Outcome Measures
NameTimeMethod
Interleukin 1. Timepoint: Before the intervention and the end of the fourth week after the start of the intervention. Method of measurement: Venous blood sample.;Interleukin 6. Timepoint: Before the intervention and the end of the fourth week after the start of the intervention. Method of measurement: Venous blood sample.
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