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Effect of intermittent fasting on blood microbiota

Effect of intermittent fasting on blood microbiota

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094470
Enrollment
Unknown
Registered
2024-12-23
Start date
2024-12-30
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

None

Interventions

Experimental group:Intermittent fasting

Sponsors

First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Have experienced more than 12 hours of fasting within at least the past year and do not cause hypoglycemia; 2. 18<=age<=65; 3. 18.5<=BMI; 4. Gender is not limited; 5. Agree to sign the informed consent form; 6. Agree to provide blood, feces, saliva, hair and urine according to the experimental design, and agree to fill in the questionnaire independently or cooperate with the questionnaire.

Exclusion criteria

Exclusion criteria: 1.History of hypoglycemia; 2.The fasting blood glucose value of the enrollment should not be lower than or beyond the normal range [3.9~6.1 mmol/L]; 3.Medication (including hypoglycemic drugs such as insulin and metformin, etc.); 4.Alcohol consumption one month before and during the experiment; 5.Take antibiotics at least 1 month before the experiment; 6.Smokers and coffee drinkers before and during the experiment; 7.Common chronic diseases such as diabetes, hypertension; 8.autoimmune diseases; Medical diseases include the mucous membranes of the digestive tract, lungs, heart, vasculature, liver, and kidneys; 9.Eating disorders (e.g. anorexia due to stress or anxiety) and abnormal eating habits (e.g. overeating and overeating at night); 10.Have any mental illness; 11.Severe hair loss and absence of hair; 12.Participation in other medical studies or fasting research projects; 12-hour fasting experience within 2 months prior to enrollment; 13.Pregnant and lactating women; 14.Subjects who have a clear travel plan during the experiment and are unable to provide a sample;

Design outcomes

Primary

MeasureTime frame
Glutamyl transferase;Aspartate aminotransferase; Alanine aminotransferase;Total cholesterol;High-density lipoprotein;Low-density lipoprotein;Triglycerides;Glycosylated hemoglobin;Insulin;Blood sugar;

Countries

China

Contacts

Public ContactZhenrong Xie

First Affiliated Hospital of Kunming Medical University

xiezhr@ydyy.cn+86 18087329011

Outcome results

None listed

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