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The evaluation of Marhame-Mafasel oinment in the treatment of patients with knee osteoarthritis

Pilot evaluation of Marhame-Mafasel ointment in patients with knee osteoarthritis: a double-blind randomized trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201126049498N2
Enrollment
66
Registered
2021-03-17
Start date
2021-03-06
Completion date
Unknown
Last updated
2021-04-26

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: Marhame-Mafasel ointment contains Arnebia euchoma as the main plant, peppermint, and chamomile essential oil. Arnebia euchroma is a perennial herbaceous plant in th

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patient satisfaction and signing of informed consent form Patients with moderate knee osteoarthritis (individuals who classified in grade 3 or moderate included moderate joint space narrowing according to Kellgren-Lawrence classification ) individuals between 40-80 years

Exclusion criteria

Exclusion criteria: Lack of cooperation of patients Patients with mild or severe knee osteoarthritis History of allergy to topical Nonsteroidal anti-inflammatory drugs (NSAIDs) Patients with a history of steroid injection into the knee joint in the past three months Consumption of oral Nonsteroidal anti-inflammatory drugs (NSAIDs) History of asthma or any liver or kidney disorders

Design outcomes

Primary

MeasureTime frame
Evaluation of ESR (Erythrocyte Sedimentation Rate). Timepoint: 1months after and before treatment. Method of measurement: Manual.;Evaluation of CRP (C-Reactive Protein). Timepoint: 1 months after and before treatment. Method of measurement: Quantitative method with diagnostic kit.;Evaluation of Rheumatoid Factor (RF). Timepoint: 1 months after and before treatment. Method of measurement: Quantitative method with diagnostic kit.;Assay of TNF-a (Tumor necrosis factor a). Timepoint: 1 months after and before treatment. Method of measurement: ELISA method.;Assay of Interleukin 6 (IL-6). Timepoint: 1 months after and before treatment. Method of measurement: ELISA method.;Evaluation of WOMAC questionnaire or Western Ontario and McMaster Universities Osteoarthritis Index to measure and determine the severity of the disability. Timepoint: 1 months after and before treatment. Method of measurement: Questionnaire.;Evaluation of visual analog scale (VAS). Timepoint: 1 months after and before treatment. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Evaluation of World Health Organization Quality of Life-BREF (WHOQOL-BREF). Timepoint: 1 months after and before treatment. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh Mizani

Shahed University

azadeh.mizani@yahoo.com+98 21 6641 8331

Outcome results

None listed

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