- 영문명
- Efficacy of ID-GMG001 for the Alleviation of Hangover: A Randomized, Double-blind, Placebo-controlled, Crossover Human Study
- 발행기관
- 대한약학회
- 저자명
- 김민철(Min Cheol Kim) 박하영(Ha-Young Park) 박종미(Jongmi Park) 임현정(Hyunjung Lim) 박주현(Ju Hyun Park) 전걸순(GulSoon Chun) 이동한(Dong Han Lee)
- 간행물 정보
- 『약학회지』제64권 제4호(2020년), 327~333쪽, 전체 7쪽
- 주제분류
- 의약학 > 기타의약학
- 파일형태
- 발행일자
- 2020.08.30

국문 초록
영문 초록
This randomized, double-blind, placebo-controlled, crossover human study aimed to investigate the efficacy of ID-GMG001 for the alleviation of hangover in men between the ages of 20 and 50 years. The selected subjects were randomized to an ID-GMG001 group and a placebo group. Two overnight assessments were conducted at Kyunghee University Hospital exactly one week apart and at the same time of day. The subjects ingested placebo or ID-GMG001 and then consumed alcohol 30 minutes later to induce hangover. The efficacy of ID-GMG001 for alleviating hangover was determined based on serum acetaldehyde levels over time. After the experiment, the results of 21 subjects who met the assessment criteria (per-protocol set) were analyzed. Comparisons of area under the curve (AUC; p=0.032), dose at 4 and 6 hours after alcohol consumption (p=0.001 and p=0.008, respectively), showed that serum acetaldehyde concentrations were significantly lower in the ID-GMG001 group than in the placebo group. A safety assessment revealed no serious IDGMG001- related adverse events, and no significant changes in vital signs and laboratory parameters occurred that could have affected patient safety. In conclusion, we determined that the use of ID-GMG001 before alcohol consumption effectively alleviates hangover in adults by reducing serum acetaldehyde concentrations.
목차
서 론(Introduction)
실험 방법(Experimental Methods)
결과 및 고찰(Results and Discussion)
결 론(Conclusion)
Conflict of Interest
References
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