Skip to content

Evaluation of the effect of basil oil on knee osteoarthritis

The effect of topical basil vera oil on clinical signs of knee joint osteoarthritis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200507047338N1
Enrollment
42
Registered
2021-04-22
Start date
2020-09-22
Completion date
Unknown
Last updated
2021-05-26

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

Conditions

knee Osteoarthritis. Unilateral primary osteoarthritis, unspecified knee

Interventions

Intervention 1: Control group: Piroxicam gel prepared from Rafsanjan pharmacy is used topically twice a day for three months for 3 to 5 minutes on the sore spot. Intervention 2: Intervention group1: T

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 70 Years

Inclusion criteria

Inclusion criteria: Diagnosis of knee osteoarthritis based on the criteria American College of Rheumatology, which is approved by a rheumatologist Average knee pain within 24 hours based on linear-Visually scale of pain between 4 and 7 cm Age limit between 45 and 70 years

Exclusion criteria

Exclusion criteria: Patients with inflammatory diseases, cancer, or serious illnesses Symptoms or history of liver or kidney failure Oral corticosteroids for the past 4 weeks or corticosteroid injections for the past 6 months fever Consumption of medicinal plants continuously drug using Sensitivity to basil Lack of willingness to continue participating in the study Failure to comply with the study protocol observation the side effects of basil oil Taking supplements and medications, take regular daily painkillers, and be very advanced Using of other topical medications at the use drug site Oral use of other analgesics and other compounds effective in the treatment of osteoarthritis up to 10 days before the study Skin ill or infectious disease or wound at the site of drug use Pregnancy

Design outcomes

Primary

MeasureTime frame
Average knee pain. Timepoint: Before the study, one and three months later. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Hatamian

Rafsanjan University of Medical Sciences

Mohammadhatamian974@gmail.com+98 35 3272 4703

Outcome results

None listed

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