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Effect of Fenugreek on the Treatment of Diabetes

Effect of fenugreek seed on anthropometric indicators, blood pressure, liver and kidney function, depression and anxiety in type 2 diabetic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017072732294N3
Enrollment
48
Registered
2017-08-21
Start date
2017-08-23
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

Non-insulin-dependent diabetes mellitus. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: intervention: 15 grams of powdered fenugreek seeds in doses of 5 grams three times a day between meals, dissolved in water, besides routine diabetic drugs, for 8 weeks. Intervention 2:
Treatment - Other
Treatment - Drugs
intervention: 15 grams of powdered fenugreek seeds in doses of 5 grams three times a day between meals, dissolved in water, besides routine diabetic drugs, for 8 weeks
control: routine diabetic drugs for 8 weeks

Sponsors

Vice chancellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: type 2 diabetes; 30-65 years old; at least 1 year and up to 10 year diabetic history; Body Mass Index<35 Exclusion criteria: insulin therapy; menopause or hysterectomy for women; having any certain diseases or using any certain medications other than diabetic ones; allergy to Fabaceae family herbs; using dietary supplements and other medicinal plants for at least three months prior to the study; smoking or using drugs

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hip circumference. Timepoint: baseline and 8 weeks after intervention. Method of measurement: measuring tape.;Waist circumference. Timepoint: baseline and 8 weeks after intervention. Method of measurement: measuring tape.;Blood pressure. Timepoint: baseline and 8 weeks after intervention. Method of measurement: sphygmomanometer.;Alanine Amino Transferase. Timepoint: baseline and 8 weeks after intervention. Method of measurement: blood sampling and commercial kits.;Aspartate aminotransferase. Timepoint: baseline and 8 weeks after intervention. Method of measurement: blood sampling and commercial kits.;Alkaline phosphatase. Timepoint: baseline and 8 weeks after intervention. Method of measurement: blood sampling and commercial kits.;Blood urea nitrogen. Timepoint: baseline and 8 weeks after intervention. Method of measurement: blood sampling and commercial kits.;Creatinine. Timepoint: baseline and 8 weeks after intervention. Method of measurement: blood sampling and commercial kits.;Depression. Timepoint: baseline and 8 weeks after intervention. Method of measurement: "Hospital Anxiety and Depression Scale" questionnaire.;Anxiety. Timepoint: baseline and 8 weeks after intervention. Method of measurement: "Hospital Anxiety and Depression Scale" questionnaire.

Secondary

MeasureTime frame
Lipid accumulation product index. Timepoint: baseline and 8 weeks after intervention. Method of measurement: Formula calculation.;Estimated glomerular filtration rate. Timepoint: baseline and 8 weeks after intervention. Method of measurement: Formula calculation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRahele tavakoly

Isfahan University of Medical Sciences

tavakkoli.rahele@yahoo.com+98 31 3792 3151

Outcome results

None listed

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