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Effect of Zingiber zerumbet pomade in treatment of knee arthrosis

Comparison of the Effectiveness of Zingiber zerumbet ointment with Diclofenac Gel on clinical symptoms in patients with Knee osteoarthritis: A randomized, double-blind, controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170428033670N1
Enrollment
80
Registered
2018-01-21
Start date
2018-01-31
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Osteoarthritis. Arthrosis, unspecified

Interventions

Intervention 1: zingiber zerumbet pomade, Knee local use. Dosage 1 grams per use 4 times a day. Intervention 2: Plus control group: diclofenac gel group. Knee local use. Dosage 1 grams per use4 times
Treatment - Drugs
zingiber zerumbet pomade, Knee local use. Dosage 1 grams per use 4 times a day.
Plus control group: diclofenac gel group. Knee local use. Dosage 1 grams per use4 times a day.

Sponsors

Immunology Research Center of Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public Contacthasan kiani Ahmadabadi

Shahed University

hasan-kiani@shahed.ac.ir+98 21 5121 4055

Outcome results

None listed

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