- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07705191
Effect of SugarLock® Peanut Skin Extract on Postprandial Blood Glucose Control
July 9, 2026 updated by: TCI Co., Ltd.
Assessing the Impact of SugarLock® Peanut Skin Extract on Postprandial Blood Glucose Control
The objective of this study is to investigate the effects of pre-meal supplementation with SugarLock® peanut skin extract and white kidney bean extract on reducing or delaying postprandial blood glucose elevation and glycemic fluctuations, and to evaluate their potential as nutritional supplements for postprandial glycemic management.
Study Overview
Status
Recruiting
Detailed Description
This study is a single-center, randomized 2×3 crossover human trial designed to evaluate the effect of SugarLock® peanut skin extract on postprandial glycemic regulation.
Healthy adults aged over 18 years with fasting blood glucose below 100 mg/dL and without type 1 or type 2 diabetes will be enrolled.
Each participant will complete three test visits, with at least a 48-hour washout interval, while wearing a continuous glucose monitoring system (CGM).
On each test day, after fasting for at least 10 hours, participants will consume either two peanut skin extract capsules, two white kidney bean extract capsules, or water only 15 minutes before eating white rice containing 50 g of carbohydrates.
Postprandial glucose responses will then be continuously monitored for 3 hours to assess the effects on blood glucose elevation and glycemic fluctuation.
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Fang-Pei Chen, Ph.D.
- Phone Number: 3310 +886-06-2785123
- Email: fpchen@mail.cjcu.edu.tw
Study Locations
-
-
-
Tainan, Taiwan, 711301
- Recruiting
- Chang Jung Christian University
-
Contact:
- Fang-Pei Chen, Ph.D.
- Phone Number: 3310 +886-06-2785123
- Email: fpchen@mail.cjcu.edu.tw
-
Principal Investigator:
- Fang-Pei Chen, Ph.D.
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Adults aged 18 years or older;
- Fasting blood glucose level < 100 mg/dL;
- Individuals without type 1 or type 2 diabetes.
Exclusion Criteria:
- Women who are pregnant, breastfeeding, or planning to become pregnant during the study period;
- Individuals with chronic gastrointestinal diseases (such as irritable bowel syndrome [IBS], inflammatory bowel disease [IBD], chronic diarrhea, celiac disease, short bowel syndrome, ulcers, colorectal cancer, etc.), a history of epilepsy or seizures, psychiatric disorders, malignant tumors, endocrine disorders, liver or kidney disease, or other major organic diseases;
- Individuals with a history of gastrointestinal surgery or organ transplantation;
- Individuals who have taken medications or supplements affecting blood glucose or insulin within the past three months;
- Individuals allergic to peanuts or white kidney beans;
- Full-time employees in the same department as the principal investigator, and students directly taught by the principal investigator during the current semester.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Blank control
consume 150 mL water 15 minutes before eating white rice containing 50 g of carbohydrates
|
consume 150 mL water
|
|
Experimental: SugarLock® peanut skin extract
consume two SugarLock® peanut skin extract capsules (200 mg/capsule) with 150 mL water 15 minutes before eating white rice containing 50 g of carbohydrates
|
consume two peanut skin extract capsules (200 mg/capsule) with 150 mL water
Other Names:
|
|
Active Comparator: White kidney bean extract
consume two White kidney bean extract capsules (250 mg/capsule) with 150 mL water 15 minutes before eating white rice containing 50 g of carbohydrates
|
consume two White kidney bean extract capsules (250 mg/capsule) with 150 mL water
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Interstitial fluid glucose level (mg/dL)
Time Frame: at 3 hours after eating white rice
|
Postprandial glucose responses will then be continuously monitored by continuous glucose monitoring system (CGM) for 3 hours
|
at 3 hours after eating white rice
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Fang-Pei Chen, Chang Jung Christian University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 9, 2026
Primary Completion (Estimated)
September 30, 2026
Study Completion (Estimated)
October 31, 2026
Study Registration Dates
First Submitted
July 9, 2026
First Submitted That Met QC Criteria
July 9, 2026
First Posted (Actual)
July 15, 2026
Study Record Updates
Last Update Posted (Actual)
July 15, 2026
Last Update Submitted That Met QC Criteria
July 9, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- A-ER-115-167
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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