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Clinical Trials in Taiwan / NCT07089732
Starting soon Not applicable

Effects of a GLP-1 Formula Drink on Gut Microbiota and Glycemic Control in Prediabetic Individuals

NCT07089732 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2025-08-08
Last updated
2025-07-28

Condition(s) studied

ObesityPrediabetes

Investigational drug(s) / intervention(s)

GLP-1 formula liquid drinkPlacebo

GLP-1 formula liquid drink: One glass jar (50 g) of the GLP-1 formula liquid drink was administered once daily, 30 minutes prior to the first meal of the day.

Placebo: One glass jar (50 g) of the placebo liquid drink was administered once daily, 30 minutes prior to the first meal of the day.

Study summary

A clinical human dietary intervention trial was conducted to investigate the effects of GLP-1 FORMUL liquid supplementation in individuals with prediabetes or obesity, with a focus on improvements in glycemic and lipid parameters, body composition, and gut microbiota profiles.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Adults aged 18 to 70 years. * Clinically diagnosed with prediabetes (fasting plasma glucose: 100-125 mg/dL or HbA1c: 5.7-6.4%) or with a body mass index (BMI) of 25-34.9 kg/m², male or female. * Have not participated in similar clinical studies within the past three months. * Able to comprehend the informed consent form, including the study procedures, potential risks, and benefits, and able to provide written informed consent. Exclusion Criteria: * Diagnosed with autoimmune diseases or cancer. * Diagnosed with gastrointestinal chronic diseases such as irritable bowel syndrome, inflammatory bowel disease, Crohn's disease, celiac disease, bowel control disorders, fecal incontinence, pancreatitis, peptic ulcer disease, colorectal cancer, short bowel syndrome, ulcerative colitis, lactose intolerance, or chronic diarrhea. * History of gastrointestinal surgery. * Planning pregnancy in the near future (including male partners), currently pregnant, or breastfeeding women. * Known allergy or hypersensitivity to probiotics or any of the study product ingredients. * History of major psychiatric disorders. * History of substance abuse or alcohol dependency.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chung Shan Medical University Taichung South

More Chung Shan Medical University trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07089732 on ClinicalTrials.gov ↗ ← All trials in Taiwan