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A randomized controlled trial on the effects of BESGLPSM oat hydrolyzed protein on GLP-1 secretion, satiety, and glucose-lipid metabolism indices in individuals with abnormal glucose-lipid metabolism

A randomized controlled trial on the effects of BESGLPSM oat hydrolyzed protein on GLP-1 secretion, satiety, and glucose-lipid metabolism indices in individuals with abnormal glucose-lipid metabolism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120839
Enrollment
Unknown
Registered
2026-03-20
Start date
2025-12-02
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Individuals with abnormal glucose and lipid metabolism

Interventions

Low-dose group:Containing 180mg oat hydrolyzed protein per tablet
Low-dose group:Containing 360mg oat hydrolyzed protein per tablet

Sponsors

Guangzhou Eighth People's Hospital Affiliated to Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 50 years old (inclusive of boundary values), gender not restricted; 2. 24.0 kgm^2 <= BMI <= 28.0 kg/m^2; 3. Fasting blood glucose level is between 5.6 - 7.0 mmol/L; 4. Within the past 1 month, weight change <= 3 kg; 5. Can read Chinese, can accurately understand the trial process, voluntarily participate in the trial and sign the informed consent form for the trial research; 6. Can cooperate with and participate in the follow-up time of the trial research, and promptly report one's own health condition or any changes in food, adverse reaction symptoms, be able to comply with the research requirements and time arrangements.

Exclusion criteria

Exclusion criteria: 1. Including diseases of important organs such as the heart, liver, lungs, kidneys, etc., blood diseases, tumor diseases, etc.; 2. Individuals with severe mental disorders, who cannot control their behaviors and cannot cooperate with the study; 3. Those who have taken items related to the study function (drugs, health supplements, hormones, etc.) within the last 3 months, which may affect the judgment of the results; 4. History of digestive system diseases, such as chronic gastritis, inflammatory bowel disease, irritable bowel syndrome, peptic ulcer, etc.; or those who have a history of gastrointestinal surgery; 5. Individuals with allergic constitution or who may be allergic to the components of the test product; 6. Pregnant women, those planning to get pregnant or breastfeeding women; 7. Those who have participated in or are currently participating in other clinical studies within the last 3 months; 8. Individuals judged by the researcher to be unsuitable for this trial or who are prone to drop out.

Design outcomes

Primary

MeasureTime frame
Body composition: height, weight, BMI, waist circumference;Glucagon-like peptide-1 (GLP-1);Plasma peptide YY (PYY) and ghrelin levels;Insulin resistance index;Lipid profile four items;VAS scale assessment of satiety;

Secondary

MeasureTime frame
Vital signs;General condition (including mental status, sleep, diet, bowel and bladder function, blood pressure, etc.);

Countries

China

Contacts

Public ContactHan Yajuan

Guangzhou Eighth People's Hospital Affiliated to Guangzhou Medical University

hanyajuannanfang@163.com+86 137 6339 3673

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026