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Effect of Arctium lappa root (Burdock) tea consumption on serum levels of oxidative stress markers, inflammatory markers, lipid profile and clinical symptoms in patient with knee osteoarthritis

Effect of Arctium lappa root (Burdock) tea consumption on serum levels of oxidative stress markers, inflammatory markers, lipid profile and clinical symptoms in patient with knee osteoarthritis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201305274105N13
Enrollment
42
Registered
2013-06-29
Start date
2013-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

knee OA. Bilateral primary osteoarthritis of knee

Interventions

Intervention 1: Arctium lappa root (Burdock) tea daily, for 6 weeks as well as physiotherapy (20 an-hour sessions for both knees), Acetaminophen 500mg twice a day, and Glucosamine one tablet daily for
Treatment - Other
Treatment - Drugs
Arctium lappa root (Burdock) tea daily, for 6 weeks as well as physiotherapy (20 an-hour sessions for both knees), Acetaminophen 500mg twice a day, and Glucosamine one tablet daily for 6 weeks
control: Physiotherapy (20 an-hour sessions for both knees) as well as Acetaminophen 500mg twice a day and Glucosamine one tablet daily for 6 weeks

Sponsors

Vice chancellor for Research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 50-70years old; primary bilateral knee osteoarthritis based on ACR criteria; ability to consume arctium lappa tea . Exclusion criteria: grade IV osteoarthritis; secondary OA; active synovitis; knee surgery or intra-articular injection; neuromuscular diseases; diabetes; metabolic diseases; cardiovascular diseases; hepatic diseases; smoking; alcohol and MI.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain, joint stiffness and Disability. Timepoint: Before and 6 weeks after the intervention. Method of measurement: Knee injury Osteoarthritis Outcome Score (KOOS) questionnaire.;Timed up and go test. Timepoint: Before and 6 weeks after the intervention. Method of measurement: based on walking time.;Visual Analog Scale (VAS). Timepoint: Before and 6 weeks after the intervention. Method of measurement: based on line.;Inflammatory markers (IL-6). Timepoint: Before and 6 weeks after the intervention. Method of measurement: Elisa.;Hs-crp. Timepoint: Before and 6 weeks after the intervention. Method of measurement: Imonoturbidometry.;Markers of Lipidemia. Timepoint: Before and 6 weeks after the intervention. Method of measurement: Espectrophotometry(mg/dl).;Measurement of serum MDA. Timepoint: Before and 6 weeks after the intervention. Method of measurement: spectrophotometry.;Erythrocyte SOD activity. Timepoint: Before and 6 weeks after the intervention. Method of measurement: spectrophotometry.;Erythrocyte GPX activity. Timepoint: Before and 6 weeks after the intervention. Method of measurement: spectrophotometry.;Serum total antioxidant capacity. Timepoint: Before and 6 weeks after the intervention. Method of measurement: spectrophotometry.

Secondary

MeasureTime frame
Physical activity. Timepoint: Before and 6 weeks after the intervention. Method of measurement: physical activity Questionnaire.;Macronutrients intake. Timepoint: Before and 6 weeks after the intervention. Method of measurement: 24-h recall Questionnaire.;Anthropometric index(weight and Body Mass Index). Timepoint: Before and 6 weeks after the intervention. Method of measurement: Analogue scale for weight and weight(Kg)/Square Height for body mass index.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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