Human Clinical Trial Evaluating the Blood Glucose-Regulating Effects of Momordica Charantia Peptides
Prediabetes is a metabolic condition characterized by elevated blood glucose levels that are higher than normal but below the diagnostic threshold for diabetes. Early intervention to improve glycemic control may help delay the progression to type 2 diabetes. Momordica charantia (bitter melon) peptides have been reported to possess potential glucose-regulating effects. This study aims to evaluate the effects of BmpP® bitter melon peptide supplementation on glycemic control in adults with prediabetes. This study is designed as a 12-week single-arm, open-label clinical trial. Approximately 12 adults aged 30-65 years with prediabetes will be recruited. Participants will consume bitter melon peptide capsules three times daily before meals for 12 weeks. Primary outcomes include fasting blood glucose, postprandial glucose response, and HbA1c levels. The findings of this study may provide preliminary evidence regarding the potential role of bitter melon peptides in blood glucose regulation.
• Adults aged 30-65 years, both male and female.
• Participants meeting any of the following criteria for prediabetes:
‣ Fasting blood glucose 100-125 mg/dL
⁃ HbA1c 5.7-6.4%
⁃ Previous clinical records indicating 2-hour OGTT glucose levels of 140-199 mg/dL
• Body mass index (BMI) between 24-35 kg/m², with waist circumference recorded (men ≥90 cm; women ≥80 cm).
• Stable lifestyle (including diet, physical activity, and sleep habits) during the past three months.
• No use of blood glucose-regulating supplements prior to or during the study.
• Willingness to comply with study procedures and complete all required assessments.
• Provision of written informed consent.