Intervention Study on Probiotic Combination Tableted Candy Hangover
Status
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Treatments
Details and patient eligibility
About
Study Design Type: Randomized, blinded, placebo-controlled, crossover trial Participants: 40 volunteers, divided into two groups (n=20) Grouping Method: Minimization randomization based on age and BMI matching
Intervention Sequence:
Group A: Probiotic intervention → washout → placebo intervention Group B: Placebo intervention → washout → probiotic intervention Blinding: Participants, data collectors, and data analysts were blinded Roles: Randomization, data collection, and data analysis were performed by different researchers
Intervention Process
Phase 1 (Week 1):
Group A: Took probiotic tablets (1g twice daily, 0.5g/tablet) Group B: Took placebo tablets (1g twice daily, 0.5g/tablet) Washout Period: 2 weeks
Phase 2 (Week 4):
Group A: Took placebo tablets Group B: Took probiotic tablets
Sample Collection
Fecal Samples: Collected at three time points:
Baseline (1 week before alcohol test) Day 7 (after Phase 1) Day 28 (after Phase 2) Alcohol Tests: Conducted on Day 7 and Day 28 after overnight fasting Body Weight: Measured on test days; alcohol dosage adjusted accordingly (1 mL/kg, 40% v/v) Serum and Saliva: Collected at multiple time points post-alcohol consumption
Full description
A randomized, blinded, placebo-controlled, crossover trial was conducted. Forty participants were divided into two groups (n=20). Then, for each block, randomization was performed by minimization by matching age and body mass index (BMI). The two groups received different sequences of Probiotic combination intervention and maltodextrin intervention (placebo), coded as A and B to conceal their identities. Participants, data collectors, and data analysts were blinded throughout the study. Different researchers performed randomization, data collection, and data analysis.
The 40 volunteers recruited were randomly divided into two groups (n=20) after signing the informed consent form, namely the Probiotic combination intervention group (Group A, probiotic intake → flushing → placebo intake) and the maltodextrin (placebo) group (Group B, placebo intake → flushing → probiotic intake). Group A tried the compressed tablet product for 1 week, and Group B tried the placebo for 1 week; after a 2-week washout period, Group A tried the placebo for 1 week, and Group B tried the compressed tablet product for 1 week. During the intervention period, volunteers took 1g of the compressed tablets twice a day (0.5g/tablet, 2 tablets) in the morning, noon and evening, and during the intervention period, volunteers took 1g of the placebo twice a day (0.5g/tablet, 2 tablets) in the morning and evening. Feces of all volunteers were collected one week before the alcohol experiment (first time), and the second and third feces were collected on the 7th and 28th days, respectively. Alcohol tests were performed on the 7th and 28th days after an overnight fast. Body weight was measured on the test day, and liquor was provided according to body weight. Participants ate a meal (standard diet) containing alcohol (alcohol content: 40% v/v, 1 mL/kg body weight), and serum and saliva of volunteers were collected at different time points after the meal. During the intervention period, all subjects followed their original dietary habits and stopped taking other alcohol-detoxifying and liver-protecting drugs or drugs that may affect alcohol metabolism. The medication method during the alcohol test was: 2 pills before the alcohol tolerance test after lunch (the first time point); 2 pills before drinking (i.e., before the hangover test at two time points); and 2 pills after waking up.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Age: 18-60 years old
- BMI: 18-25 kg/m2
- Healthy adults with experience of being drunk, fully understanding the experimental plan, and voluntarily agreeing to participate
- Able to tolerate a certain amount of alcohol (calculated as 60 kg, about 60 mL of 40-proof liquor)
- Must be able to swallow tablets
Exclusion criteria
- People who are very intolerant to alcohol, with aldehyde dehydrogenase activity of 2%
- People with a history of allergic reactions or clinical allergic reactions to drugs, alcohol, products or other ingredients
- People who have taken drugs that induce and inhibit drug metabolizing enzymes, such as barbiturates, within one month from the date of the screening test
- People who have taken drugs that affect the results of clinical trials (alcohol metabolism) (aspirin, antipyretics, anti-inflammatory drugs, analgesics, antibiotics, herbal medicines, oral steroids, hormones, etc.) within 1 month from the screening population
- People who have taken drugs, products and functional foods that affect the intestines (such as probiotics, yogurt, etc.) within 10 days before the test
- People who have taken drugs, products or functional foods that have a functional effect on the stomach and liver within 10 days before the test
- People who have taken drugs, products or functional foods that have a functional effect on the stomach and liver within 10 days before the test. Those who have taken products that affect the test results, such as products or drugs that relieve alcohol, etc.
- Those who suffer from severe acute or chronic diseases such as cardiovascular disease, metabolic disease, hepatobiliary disease, pancreatic disease, muscle disease, nervous system disease, mental disorder, endocrine disease, immune disease, kidney disease, malignant tumor, lung disease and other diseases that require treatment
- Those who have received or are receiving clinically significant treatment for gastrointestinal diseases such as gastric or duodenal ulcers
- Those who have donated blood within 2 months from the date of screening
- Those whose serum AST, ALT or creatine kinase levels are higher than the reference range or twice the serum upper limit, and the creatinine level in the diagnostic test exceeds 2.0 mg/dL
- Those who are considered unsuitable due to diagnostic test results or other reasons.
Trial design
Primary purpose
Allocation
Interventional model
Masking
40 participants in 2 patient groups, including a placebo group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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