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Evaluation the effect of fenugreek on reducing blood lipids

Evaluation the effect of the fenugreek hydrolyzed protein on lipids and CRP levels in hypercholesterolemia patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210125050142N1
Enrollment
60
Registered
2021-03-11
Start date
2021-04-04
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Hypercholesterolemia.

Interventions

Intervention 1: Intervention group: Patients in this group will be prescribed a 40 gram capsule of fenugreek hydrolyzed protein daily for 2 months. Lipid profile, hs-CRP level, fasting blood sugar, bl

Sponsors

National institute for medical research development
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with low to moderate risk for cardiovascular events LDL 116 -180 mg /dL

Exclusion criteria

Exclusion criteria: Drinking alcohol, Use of effective supplements on blood lipids (such as fish oil), Immunosuppressive drugs, blood lipid-lowering drugs (statins, fibrates, niacin, …) People with hypothyroidism, nephrotic syndrome or renal dysfunction or liver dysfunction People with uncontrolled hypertension (systolic blood pressure greater than 160 or diastolic blood pressure greater than 100 mmHg), History of dizziness and convulsions, Pregnancy or lactation Sensitivity to studied plant

Design outcomes

Primary

MeasureTime frame
Mean of Total Cholesterol. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Blood level mg mg / dL by laboratory.;Mean of High-Density Lipoprotein. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Blood level mg mg / dL by laboratory.;Mean of Low-Density Lipoprotein. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Blood level mg mg / dL by laboratory.;Mean of Triglyceride. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Blood level mg mg / dL by laboratory.;Mean of high-sensitivity C-reactive protein. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Blood level mg mg / dL by laboratory.

Secondary

MeasureTime frame
Mean of fasting blood sugar. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Blood level mg mg / dL by laboratory.;Mean of blood pressure. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Blood pressure monitor.;Mean of body mass index. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Tape meters, digital scales and calculation formulas.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdi Badiee Gavarti

Esfahan University of Medical Sciences

badiee9675@gmail.com+98 31 3577 0701

Outcome results

None listed

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