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Recruiting NCT07705191

Effect of SugarLock® Peanut Skin Extract on Postprandial Blood Glucose Control

No phase Interventional Blood Sugar (Glucose) Control Postprandial Glucose

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Peanut skin extract, White kidney bean extract, Water.
Who it may be relevant to
Registry conditions: Blood Sugar (Glucose) Control, Postprandial Glucose. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

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.

Interventions

  • Dietary supplement Peanut skin extract
    consume two peanut skin extract capsules (200 mg/capsule) with 150 mL water
  • Dietary supplement White kidney bean extract
    consume two White kidney bean extract capsules (250 mg/capsule) with 150 mL water
  • Dietary supplement Water
    consume 150 mL water

Primary outcome measures

  • Interstitial fluid glucose level (mg/dL) [Time frame: at 3 hours after eating white rice]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Open label
Primary purpose
Treatment

Study locations

Taiwan · 1 center
  • Chang Jung Christian University — Tainan

Identifiers

NCT: NCT07705191 · A-ER-115-167

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗