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NCT Number: NCT07705191

Effect 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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Chang Jung Christian University

Tainan, 711301, Taiwan

Location status: Recruiting

Location contact

Fang-Pei Chen, Ph.D.

CONTACT

[email protected]

+886-06-2785123 ext. 3310

Fang-Pei Chen, Ph.D.

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Peanut skin extract

Dietary Supplement

consume two peanut skin extract capsules (200 mg/capsule) with 150 mL water

Other names: SugarLock®

White kidney bean extract

Dietary Supplement

consume two White kidney bean extract capsules (250 mg/capsule) with 150 mL water

Water

Dietary Supplement

consume 150 mL water

Primary outcomes

  1. 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

Study contacts

Contact information is provided by the study sponsor or research team.

Fang-Pei Chen, Ph.D.

CONTACT

[email protected]

+886-06-2785123 ext. 3310

Sponsors and collaborators

Lead sponsor

TCI Co., Ltd.

Industry

Registry information

Official study title

Assessing the Impact of SugarLock® Peanut Skin Extract on Postprandial Blood Glucose Control

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 15, 2026
Registry last updated
Jul 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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