The effect of long-term Momordica Charantia supplementation on blood glucose levels
- Conditions
- blood glucosepre-diabetes10018424
- 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
• Age 40-75yrs
• BMI >25 kg/m2
• Having a fasting glucose >= 5.6 mmol/L
• 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
Name Time Method <p>The main study parameter is fasting levels of plasma glucose. </p><br>
- Secondary Outcome Measures
Name Time Method <p>-</p><br>
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