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Effects of Arctium Lappa root in individuals with type 2 diabetes

Effects of Arctium Lappa root on values of blood sugar, amylase, antioxidants, lipid ratios and insulin resistance in individuals with type 2 diabetes

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210222050455N1
Enrollment
80
Registered
2021-04-22
Start date
2021-04-04
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

type 2 diabetes. Diabetes mellitus due to underlying condition

Interventions

Intervention 1: Intervention group: One capsule Arctium Lappa root (460 mg) per day for 12 weeks. Intervention 2: Control group: One capsule placebo charcoal (460 mg) day for 12 weeks.

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: Diagnosis of type 2 diabetes over two years (FBS>125 ? 2hpp>200 ? HbA1c>6/5 ) No change in the dose of oral blood glucose lowering during testing Maintain physical activity and diet as usual during the test No liver, gastrointestinal and kidney diseases Lack of treatment with anticoagulants Do not take anti hypertensive drugs and diuretics No alcohol No smoking No allergies

Exclusion criteria

Exclusion criteria: People who receive vitamin supplements during the last three months People treated with insulin and other hormones People who are pregnant and breastfeeding

Design outcomes

Primary

MeasureTime frame
Fasting glucose. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Colorimetric.;Amylase. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Spectrophotometry.;Catalase. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Spectrophotometry.;MDA. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Calorimetry.;Total antioxidant capacity (TAC). Timepoint: Before and after 12 weeks of intervention. Method of measurement: Calorimetry.;Insulin. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Eliza.;HbA1C. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Calorimetry.;Lipid profile. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Calorimetry.;Lipid ratios(Total Cholesterol/HDl-c and LDL-c/HDl-c). Timepoint: Before and after 12 weeks of intervention. Method of measurement: Formula.;HOMA-B. Timepoint: Before and after 12 weeks of intervention. Method of measurement: HOMA-IR model evaluation.

Secondary

MeasureTime frame
Body mass index (BMI). Timepoint: Before and after 12 weeks of intervention. Method of measurement: weight/height.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoume Ghorbani

Arak University of Medical Sciences

M.ghorbani7133@gmail.com+98 86 3417 3501

Outcome results

None listed

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