Skip to content

The effect of a topical product prepared from mustard seed oil in patients with knee osteoarthritis

Evaluation the effect of a topical product prepared from mustard seed oil in controlling pain and improving the performance of patients with knee osteoarthritis, a double-blind randomized controlled clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220812055668N1
Enrollment
30
Registered
2022-11-16
Start date
2022-10-02
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

knee osteoarthritis. Osteoarthritis of knee

Interventions

Intervention 1: Intervention group: Patients who underwent intra-articular injection of Hyaluronic Acid (Hyaluronic Acid Sodium salt 2%) called vijoint one (in the form of a ready-to-inject 60mg/3ml s

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: The study is conducted on patients referred to the pain clinic of Imam Reza (AS) Shiraz With the initial complaint of "knee pain" which has been confirmed as "osteoarthritis of the knee joint" in radiological examination and imaging The age range of patients is between 40 and 80 years Patients with ASA class I, II are included in the study The grade of knee abrasion should be grade II-III based on radiological imaging

Exclusion criteria

Exclusion criteria: Patients with the following underlying diseases are excluded from the study diabetes Connective tissue diseases Peripheral vascular diseases Alzheimer All kinds of diseases and movement disorders of the lower limbs Psychiatric diseases

Design outcomes

Primary

MeasureTime frame
Knee pain. Timepoint: Before the intervention, 4 weeks and 12 weeks after starting to use the topical product of mustard seed oil. Method of measurement: Changes in scores of VAS and WOMAC questionnaires.;Joint dryness. Timepoint: Before the intervention, 4 weeks and 12 weeks after starting to use the topical product of mustard seed oil. Method of measurement: Changes in WOMAC questionnaire scores.;Patient functionality. Timepoint: Before the intervention, 4 weeks and 12 weeks after starting to use the topical product of mustard seed oil. Method of measurement: Changes in WOMAC questionnaire scores.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Mehdi Zarshenas

Shiraz University of Medical Sciences

zarm@sums.ac.ir+98 917 117 3491

Outcome results

None listed

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