Human trials to evaluate the usefulness and safety of CKDHC hangover intake hangover improvement
- Conditions
- Not Applicable
- Registration Number
- KCT0004554
- Lead Sponsor
- ChongKunDang Healthcare
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Persons who meet all of the following conditions are selected as subjects for human application.
1) Men and women over 19 years old and under 40 years old
2) Those who have had a hangover after drinking alcohol
3) Those who consumed more than 1 bottle of soju and less than 3 bottles a week in the past month (based on 17 degrees of soju)
4) A person who agrees to participate in the human body application test and writes informed consent before the test starts.
Persons subject to one or more of the following conditions are excluded from human subjects.
1) Those who have a history of severe malignant tumors, cerebrovascular diseases (cerebral infarction, cerebral hemorrhage, etc.), and heart diseases (angina, myocardial infarction, heart failure, arrhythmia requiring treatment) within the last 6 months. Stable subjects may participate in the study at the discretion of the principal investigator.)
2) Patients with peptic ulcer and reflux esophagitis
3) Those who have had past gastric acid suppression or gastroesophageal surgery
4) Alcohol use disorders or alcoholics
5) Those who have drunk enough to interfere with the test within one week of the test
6) Those who are continuously taking drugs that are likely to affect alcohol metabolism, aspirin, steroid bleeding, nonsteroidal drugs, or painkillers
7) Those who have taken medicines and functional foods related to liver function improvement within 2 weeks of the start of the test
8) Those with liver function abnormalities
9) Those with new function abnormalities
10) thyroid disease
11) Patients with uncontrolled hypertension (more than 160mmHg systolic blood pressure or more than 100mmHg diastolic blood pressure, measured after 10 minutes of test subjects)
12) Diabetics with uncontrolled blood sugar through investigation of medication and medical history
13) Those who are pregnant or plan to become pregnant during this human testing period.
14) Participation in another clinical trial within one month or plan to participate in another clinical trial during this human trial.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood alcohol (blood, exhalation), acetaldehyde concentration;Hangover Symptom Questionnaire
- Secondary Outcome Measures
Name Time Method Vital signs (blood pressure, pulse), weight