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The effect of Portulaca oleracea capsule on knee osteoarthritis

Clinical trial of Portulaca oleracea extract capsule on clinical indicators of osteoarthritis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190406043175N5
Enrollment
80
Registered
2021-08-30
Start date
2021-10-23
Completion date
Unknown
Last updated
2021-08-30

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: Portulaca oleracea capsule (prepared in Pharmacological Research Center of Medicinal Plants) three times a day, and routine treatment with meloxicam tablets. Interv

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Initial symptomatic osteoarthritis in at least one knee by clinical or radiological criteria ACR (American College of Rheumatology) is approved Lack of proper adherence to routine drug treatment (meloxicam tablets) for at least two weeks before the study Score higher than 30 at baseline VAS scale

Exclusion criteria

Exclusion criteria: The intra-articular injection of hyaluronic acid in the three months before the start of the study The 4-week treatment with oral corticosteroids before the start of the study Patients with a history of deep vein thrombosis Active liver or renal disease and malignancies Secondary osteoarthritis or suspected Patients treated with hormonal drugs Patients treated with anticoagulation drugs Patients with a history of ischemic or hemorrhagic stroke

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Early intervention, four weeks after the intervention, eight weeks after intervention. Method of measurement: Western Ontario and McMasters Universities Osteoarthritis Index (Womac) questionnaire and Visual Analog Scale (VAS) scale.;Joint stiffness. Timepoint: Early intervention, four weeks after the intervention, eight weeks after intervention. Method of measurement: (Womac) questionnaire and (VAS) scale.;Physical performance. Timepoint: Early intervention, four weeks after the intervention, eight weeks after intervention. Method of measurement: (Womac) questionnaire and (VAS) scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Forouzanfar

Mashhad University of Medical Sciences

forouzanfarf@mums.ac.ir+98 51 3800 2538

Outcome results

None listed

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