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Effects on Blood Glucose Fluctuations of Eating Order of Different Food Ingredients Detected by Freestyle Libre Flash Glucose Monitoring System in Patients with Abnormal Glucose Metabolism

Effects on Blood Glucose Fluctuations of Eating Order of Different Food Ingredients Detected by Freestyle Libre Flash Glucose Monitoring System in Patients with Abnormal Glucose Metabolism

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021792
Enrollment
Unknown
Registered
2019-03-09
Start date
2019-03-11
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

diabetes

Interventions

Group 3:different diet order
impaired glucose tolerance:different diet orders
diabetes:different diet order

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. aged 14-70 years old male and female; 2. All participants agree to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Diabetic patients with poor blood glucose control: HbA1c >9.5%; 2. Use of drugs that may affect the outcome measures of this study 1 months before enrollment, including pioglitazone, GLP-1 receptor agonist, DPP-4 inhibitor, insulin, and glycyrrhizic acid preparation, etc; 3. Accompanied by other diseases that affect glucose and lipid metabolism, such as hypothyroidism, hyperthyroidism, hypercortisolism, etc; 4. Accompanied by severe liver diseases caused by viral hepatitis, drugs, auto-immune hepatitis, hereditary liver disease, liver cirrhosis, liver cancer, etc; 5. Accompanied by biliary tract diseases, biliary obstructive disease, etc; 6. Accompanied by chronic kidney disease or severe renal impairment, defined as serum creatinine greater than 2.0mg/dL (176.8umol/L); 7. Life expectancy is no more than 5 years; 8. Pregnant or planning to become pregnant recently for female participant; 9. There is a chewing dysfunction or eating disorder; 10. Allergic to some food, or for alcohol or iodine using for skin disinfection; 11. Can't accept indwelling needles in the body; 12. Any situation that may affect the implementation or results of the study; 13. Subjects participated in other clinical trials in the past 4 weeks; 14. The researchers think they were unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
postprandial blood glucose;

Secondary

MeasureTime frame
glucose excursion;HbA1c;

Countries

China

Contacts

Public ContactHongmei YAN

Zhongshan Hospital, Fudan University

yan.hongmei@zs-hospital.sh.cn+86 13761666976

Outcome results

None listed

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