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The effect of long-term Momordica Charantia supplementation on blood glucose levels

Conditions
blood glucose
pre-diabetes
10018424
Registration Number
NL-OMON51413
Lead Sponsor
Wageningen Food and Biobased Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

• Age 40-75yrs
• BMI >25 kg/m2
• Having a fasting glucose >= 5.6 mmol/L

Exclusion Criteria

• Use of medication/supplements that may influence the study results, such as
metformin, gliclazide, glimepiride, tolbutamide, insulin, sitagliptin (DPP4
inhibitor), liraglutide (GLP-1 agonist), acarbose, repaglinide, pioglitazone,
corticosteroids (systemically) , SGLT-2 inhibitors, (judged by our research
physician)
• Having a fasting glucose >11.0 mmol/L
• History of gastro-intestinal surgery or having (serious) gastro-intestinal
complaints
• History of liver dysfunction (cirrhosis, hepatitis) or liver surgery
• Kidney dysfunction (self-reported)
• Reported slimming, medically prescribed or other extreme diets
• Reported weight loss or weight gain of > 5 kg in the month prior to pre-study
screening
• Not willing to give up blood donation during the study
• Current smokers
• Alcohol intake >=14 glasses (women) or >21 glasses (men) of alcoholic
beverages per week, on average
• Not pregnant or lactating
• Abuse of illicit drugs (soft- and hard drugs)
• Food allergies for products that we use in the study
• Participation in another clinical trial at the same time
• Being an employee of the Food, Health & Consumer Research group of Wageningen
Food & Biobased Research or dept. human nutrition and health of Wageningen
University.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main study parameter is fasting levels of plasma glucose. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>-</p><br>
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