Actively Recruiting
Effects of GLP-1 Formula on GLP-1 and Glucose Regulation
Led by Shih Chien Huang · Updated on 2025-07-24
100
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
Sponsors
S
Shih Chien Huang
Lead Sponsor
T
TCI Co., Ltd.
Collaborating Sponsor
AI-Summary
What this Trial Is About
This clinical trial is designed to evaluate the physiological effects of a GLP-1 Formula on glucagon-like peptide-1 (GLP-1) secretion and glycemic regulation in adults with elevated body fat percentage. The GLP-1 Formula is a multi-component dietary supplement composed of Bifidobacterium breve (probiotic), ClpB Formula-a prebiotic blend containing probiotic kombucha extract, soy peptide powder, L-arabinose, and erythritol-and rocket apple extract. The study consists of two randomized crossover trials: Trial 1 (n = 50) aims to assess the effects of the formula on circulating GLP-1 concentrations, while Trial 2 (n = 50) investigates its impact on blood glucose and insulin responses. Eligible participants will be healthy adults aged 18 to 50 years with a body fat percentage greater than 25%, recruited via institutional and online outreach. Participants may choose to enroll in either or both trials; if enrolled in both, a washout period of at least one month between trials is required. Each trial consists of two intervention visits following a crossover design, with supplementation switched on day 8. Each visit will last approximately 6 hours, during which physiological and biochemical assessments will be conducted. Primary outcome measures include plasma levels of GLP-1, glucose, and insulin; secondary outcomes include appetite-related indices. This study aims to elucidate the potential of this functional formula to modulate incretin response and glycemic homeostasis in individuals with elevated adiposity.
CONDITIONS
Official Title
Effects of GLP-1 Formula on GLP-1 and Glucose Regulation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female participants aged 18-50 years
- Body fat percentage greater than 25%
You will not qualify if you...
- Use of probiotics, weight loss products, or gastrointestinal supplements or medications within the past month
- Presence of diabetes, autoimmune diseases, cancer, chronic gastrointestinal disorders, lactose intolerance, or chronic diarrhea
- History of gastrointestinal surgery
- Pregnant or breastfeeding women
AI-Screening
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Trial Site Locations
Total: 1 location
1
Chung Shan Medical University Hospital
Taichung, Taiwan, 402
Actively Recruiting
Research Team
S
Shih-Chien Huang, PhD, Associate Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
PREVENTION
Number of Arms
2
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