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The effect of topical Pistacia vera oil on knee joint osteoarthritis

The effect of topical Pistacia vera oil on clinical signs and symptom of knee joint osteoarthritis: a randomized and double blind clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180811040759N1
Enrollment
75
Registered
2019-09-09
Start date
2019-03-21
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Osteoarthritis. Osteoarthritis of knee

Interventions

Intervention 1: Intervention group: Group A is used topically in the pyroxicam gel. The treatment duration is 3 months and twice daily. During the study, patients are only allowed to use oral analgesi

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 70 Years

Inclusion criteria

Inclusion criteria: age 45-70 years diagnosis of knee osteoarthritis according to American College of Rheumatology, approved by rheumatology specialist the average knee pain within 24 hours is based on the linear-visual pain scale (VAS) between 4 to 7

Exclusion criteria

Exclusion criteria: Patients with inflammatory diseases (such as lupus, rheumatoid arthritis, history of brucellosis, etc.) cancer or chronic diseases symptoms or history of liver or kidney failure oral corticosteroid consumption during the past 4 weeks corticosteroid injection in the last 6 months fever Consumption of medical herbs continuously Smoking pistachio allergy use of food and drug supplements Oral use of other analgesics and other compounds effective in treating osteoarthritis up to 10 days before the study Skin or infectious disease or ulcer at the place of administration pregnancy

Design outcomes

Primary

MeasureTime frame
Knee pain intensity. Timepoint: At the beginning and the end of the study (three months after the beginning of the study). Method of measurement: The linear-visual scale of pain.;Morning stiffness & Patients' function. Timepoint: At the beginning and the end of the study (three months after the beginning of the study). Method of measurement: WOMAC questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme nazhadkoorki

Rafsanjan University of Medical Sciences

fatemenezhadi@gmail.com+98 34 3428 0038

Outcome results

None listed

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