Bitter melon peptide supplement tested for prediabetes blood sugar control
NCT ID NCT07504029
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether bitter melon peptide capsules can help control blood sugar in adults with prediabetes. About 12 people aged 30-65 will take the capsules three times daily before meals for 12 weeks. Researchers will measure blood sugar and HbA1c levels to see if the supplement improves glycemic control.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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30 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 30-65 years, both male and female. * Participants meeting any of the following criteria for prediabetes: 1. Fasting blood glucose 100-125 mg/dL 2. HbA1c 5.7-6.4% 3. 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. Exclusion Criteria: * Diagnosis of type 2 diabetes mellitus (HbA1c ≥6.5% or physician diagnosis). * Current use of antidiabetic medications (e.g., metformin, DPP-4 inhibitors, SGLT2 inhibitors, GLP-1 receptor agonists, or insulin). * Use of medications that may affect blood glucose levels, such as corticosteroids, antipsychotic drugs, or unstable thyroid medications. * Presence of severe hepatic, renal, cardiovascular diseases, active cancer, or gastrointestinal malabsorption disorders. * Pregnant or breastfeeding women, or those planning to become pregnant. * Body weight change exceeding ±5% within the past three months, or currently following a weight-loss program or special diet. * History of alcohol abuse or substance misuse. * Individuals engaged in night shift or rotating shift work. * Known allergy to any component of the study product. * Participation in another clinical trial within the past 1 month, or antibiotic use within the past 8 weeks (if gut microbiota analysis is involved). * Individuals who are students currently taught by Associate Professor You-Cheng Shen or Dr. Jing-Bin Lin, or laboratory staff, assistants, or employees with a supervisory or subordinate relationship with the investigators.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
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Contacts and locations
Locations
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Chung Shan Medical University
RECRUITINGTaichung, Taiwan