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A clinical trial of the determination of glycemic index (GI) of Baishanping full nutrition formula food for special medical purpose for diabetics

A clinical trial of the determination of glycemic index (GI) of Baishanping full nutrition formula food for special medical purpose for diabetics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112664
Enrollment
Unknown
Registered
2025-11-18
Start date
2025-11-21
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Diabetes

Interventions

Experimental group:The subjects were measured after three independent meals which were reference food, test food, and reference food. The interval between each independent meal measurement was >= 72 h

Sponsors

JingJiang Pepole’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Peopele who are healthy adults (between 18 and 60 years old) with half male and half female, non pregnant and lactating women, and need to meet the following physical examination items within the normal range: blood glucose (fasting blood glucose, insulin, C-peptide, glycated hemoglobin), blood pressure, blood lipids, routine blood test,routine urine test, liver function test, renal function test, electrocardiogram examination. 2.Body mass index(BMI) between 18.5~24.0kg/m^2. 3.No history of diabetes (or impaired glucose tolerance), no other metabolic disease, digestive system disease, endocrine system disease, mental disease, etc. 4.No history of food allergies and intolerance. 5.During the past 3 months,no taking nutritional supplements that affect glucose tolerance,oral contraceptives, acetylsalicylic acid, steroids, protease inhibitors and anti psychotic drugs. 6.Can tolerate fasting state for at least 10 hours.

Exclusion criteria

Exclusion criteria: 1.People who do not meet the inclusion criteria, such as medical examination reports that do not meet the requirements, or other reasons that are not suitable for participating in this clinical study, such as difficulty in blood collection, dizziness with needles and blood, and inability to participate in the trial according to the research plan, etc. 2.Researchers consider it inappropriate to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Blood glucose;

Countries

China

Contacts

Public ContactWei Yang

JingJiang Pepole’s Hospital

1982918256@qq.com+86 189 6103 3232

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026