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The Effect of oral prescription of Echinops SPP and Curcumin on the Consequences of Idiopathic knee Osteoarthritis

The Effect of oral prescription of Echinops SPP and Curcumin on the Consequences of Idiopathic knee Osteoarthritis: a double blind clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110603006698N4
Enrollment
96
Registered
2021-06-23
Start date
2021-07-23
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

Primary Osteoarthritis. Primary osteoarthritis, other specified site

Interventions

Intervention 1: Take Echinops SPP. Capsules with a dose of 750 mg twice a day for 90 days. Intervention 2: Take Curcumin Capsules with a dose of 750 mg twice a day for 90 days. Intervention 3: Control

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Suffering Osteoarthritis based on physical examinations and criteria of the American Rheumatology Association, which is approved by the Iranian Rheumatology Association. Idiopathic form of osteoarthritis of the knee.3. In case of underlying disease, this disease should be under control.

Exclusion criteria

Exclusion criteria: Any unexpected event that affects the patient's continued participation in the study The patient does not want to continue participating in the study Having a serious illness that requires special medication interventions

Design outcomes

Primary

MeasureTime frame
Evaluation of multidimensional health status specific to osteoarthritis (clinical symptoms, knee joint stiffness, knee pain and knee function and daily activities). Timepoint: Pre intervention, 30 days after beginning of intervention, 90 days after beginning of intervention. Method of measurement: WOMAC (Western Ontario and MC Master Universities Arthritis Index).;Knee range of motion. Timepoint: Pre intervention, 30 days after beginning of intervention, 90 days after beginning of intervention. Method of measurement: Goniometry.

Secondary

MeasureTime frame
Knee range of motion. Timepoint: Pre intervention, 30 days after beginning of intervention, 90 days after beginning of intervention. Method of measurement: Goniometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMozhgan Behshid

Tabriz University of Medical Sciences

mozhganbehshid@hotmail.com+98 41 3479 6770

Outcome results

None listed

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