Alcohol intake
Conditions
Interventions
A Group:Participants were randomly divided into two groups. Group A subjects fasted for more than 8 hours, and blood samples were taken to measure alanine transaminase (ALT), aspartate transaminase (A
B Group:Participants were randomly divided into two groups. Group B subjects fasted for more than 8 hours, and blood samples were taken to measure alanine aminotransferase (ALT), aspartate aminotransf
Sponsors
Central Hospital of Fengxian District, Shanghai
Eligibility
Sex/Gender
All
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: (1) Subjects are between 18 and 45 years of age. (2) No alcohol consumption is allowed within 3 days prior to the experiment. (3) Participants in a clinical trial who have no significant systemic disease (including physical, mental, and social) and whose measures are within the normal measuring range or have no clinical significance in the investigator's judgment. (4) Subjects voluntarily participate in this clinical study and complete a written informed consent signature.
Exclusion criteria
Exclusion criteria: (1) There is (or has) a history of alcohol addiction. (2) He is known to be allergic to alcohol. (3) Pregnant or breastfeeding. (4) People with diabetes mellitus, hypertension.coronary heart disease, liver and kidney insufficiency, cancer, renal failure, cerebral hemorrhage, cerebral apoplexy, cardiorespiratory insufficiency, myocardial infarction, cardiac stent and artificial pacemaker. (5) Persons with mental illness and loss of ability to function autonomously.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in breath alcohol level and blood alcohol content; | — |
Secondary
| Measure | Time frame |
|---|---|
| Alanine transaminase;aspartate transaminase;blood sugar; | — |
Countries
China
Contacts
Public ContactZhang Shan
Endocrinology and Metabolism Department, Central Hospital of Fengxian District, Shanghai
Outcome results
None listed