A Randomized, Double-blind, Active-controlled Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of Goodmorning S Granule® on Constipation

Background/Aims: Constipation is a common gastrointestinal disease that reduces the quality of life and incurs considerable medical expenses. Bisacodyl and sodium docusate are generally used to treat constipation. This study assessed the effectiveness and safety of Goodmorning S Granule® (Hanpoong P...

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Published in:The Korean Journal of Gastroenterology
Main Authors: Munjin Ju, Nayoung Kim, Cheol Min Shin, Young Soo Park, Hyuk Yoon, Yonghun Choi, Dong Ho Lee
Format: Article
Language:English
Published: Jin Publishing & Printing Co. 2022-07-01
Subjects:
Online Access:https://www.kjg.or.kr/journal/view.html?uid=5834&vmd=Full
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author Munjin Ju
Nayoung Kim
Cheol Min Shin
Young Soo Park
Hyuk Yoon
Yonghun Choi
Dong Ho Lee
author_facet Munjin Ju
Nayoung Kim
Cheol Min Shin
Young Soo Park
Hyuk Yoon
Yonghun Choi
Dong Ho Lee
author_sort Munjin Ju
collection DOAJ
container_title The Korean Journal of Gastroenterology
description Background/Aims: Constipation is a common gastrointestinal disease that reduces the quality of life and incurs considerable medical expenses. Bisacodyl and sodium docusate are generally used to treat constipation. This study assessed the effectiveness and safety of Goodmorning S Granule® (Hanpoong Pharm. Co., Ltd., Wanju, Korea) in functional constipation by a comparison with bisacodyl. Methods: A 2-week randomized, double-blind, active-controlled exploratory clinical trial was conducted to compare the treatment (Goodmorning S Granule®) with the control (bisacodyl). The efficacy was measured by the changes in transition, Bristol stool type, stomachache, clinical manifestation, defecation time after drug consumption, 36-item short-form survey (SF-36), and the results of improvement evaluation. The safety was evaluated by the incidence of adverse drug events and vital signs. Additional analyses were conducted by dividing the severity according to the proportion of Bristol Stool Scale types 1 and 2. Results: Subjects were randomized to the treatment (n=24) or control (n=26) groups. No significant differences were observed in demographics. After 2 weeks from the baseline, the changes in the complete spontaneous bowel movement (CSBM) were higher in the treatment (4.00±2.62) group than in the control group (1.40±2.34) (p<0.05). The treatment group exhibited significant improvement in the score on the SF-36 questionnaire. The clinical side effects, such as stomachache and borborygmus, were reduced in the moderate constipation patients in the treatment group, according to additional analyses. Conclusions: Goodmorning S Granule®, a herbal medicine, was more effective in improving quality of life and CSBM per week and safer in the moderate constipation groups because of the reduced clinical side effects.
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spelling doaj-art-2ef637da2e2d41f5b9bc86a587e8bbc42025-08-20T00:24:00ZengJin Publishing & Printing Co.The Korean Journal of Gastroenterology1598-99922233-68692022-07-01801172710.4166/kjg.2022.025A Randomized, Double-blind, Active-controlled Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of Goodmorning S Granule® on ConstipationMunjin Ju0Nayoung Kim1Cheol Min Shin2Young Soo Park3Hyuk Yoon4Yonghun Choi5Dong Ho Lee6https://orcid.org/0000-0002-6376-410XDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, KoreaDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, KoreaDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, KoreaDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, KoreaDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, KoreaDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, KoreaDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, KoreaBackground/Aims: Constipation is a common gastrointestinal disease that reduces the quality of life and incurs considerable medical expenses. Bisacodyl and sodium docusate are generally used to treat constipation. This study assessed the effectiveness and safety of Goodmorning S Granule® (Hanpoong Pharm. Co., Ltd., Wanju, Korea) in functional constipation by a comparison with bisacodyl. Methods: A 2-week randomized, double-blind, active-controlled exploratory clinical trial was conducted to compare the treatment (Goodmorning S Granule®) with the control (bisacodyl). The efficacy was measured by the changes in transition, Bristol stool type, stomachache, clinical manifestation, defecation time after drug consumption, 36-item short-form survey (SF-36), and the results of improvement evaluation. The safety was evaluated by the incidence of adverse drug events and vital signs. Additional analyses were conducted by dividing the severity according to the proportion of Bristol Stool Scale types 1 and 2. Results: Subjects were randomized to the treatment (n=24) or control (n=26) groups. No significant differences were observed in demographics. After 2 weeks from the baseline, the changes in the complete spontaneous bowel movement (CSBM) were higher in the treatment (4.00±2.62) group than in the control group (1.40±2.34) (p<0.05). The treatment group exhibited significant improvement in the score on the SF-36 questionnaire. The clinical side effects, such as stomachache and borborygmus, were reduced in the moderate constipation patients in the treatment group, according to additional analyses. Conclusions: Goodmorning S Granule®, a herbal medicine, was more effective in improving quality of life and CSBM per week and safer in the moderate constipation groups because of the reduced clinical side effects.https://www.kjg.or.kr/journal/view.html?uid=5834&vmd=Fullconstipationlaxativesherbal medicinetreatment outcomesafety
spellingShingle Munjin Ju
Nayoung Kim
Cheol Min Shin
Young Soo Park
Hyuk Yoon
Yonghun Choi
Dong Ho Lee
A Randomized, Double-blind, Active-controlled Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of Goodmorning S Granule® on Constipation
constipation
laxatives
herbal medicine
treatment outcome
safety
title A Randomized, Double-blind, Active-controlled Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of Goodmorning S Granule® on Constipation
title_full A Randomized, Double-blind, Active-controlled Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of Goodmorning S Granule® on Constipation
title_fullStr A Randomized, Double-blind, Active-controlled Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of Goodmorning S Granule® on Constipation
title_full_unstemmed A Randomized, Double-blind, Active-controlled Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of Goodmorning S Granule® on Constipation
title_short A Randomized, Double-blind, Active-controlled Exploratory Clinical Trial for the Evaluation of the Efficacy and Safety of Goodmorning S Granule® on Constipation
title_sort randomized double blind active controlled exploratory clinical trial for the evaluation of the efficacy and safety of goodmorning s granule r on constipation
topic constipation
laxatives
herbal medicine
treatment outcome
safety
url https://www.kjg.or.kr/journal/view.html?uid=5834&vmd=Full
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