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한의약융합데이터센터


근거중심한의약 DB

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Title

Kikyo-to vs. Placebo on Sore Throat Associated with Acute Upper Respiratory Tract Infection: A Randomized Controlled Trial.

Authors

Ishimaru N, Kinami S, Shimokawa T, Kanzawa Y.

Journal

Intern Med.

Year

2019

Vol (Issue)

58(17)

Page

2459-65.

doi

10.2169/internalmedicine.2748-19.

PMID

31178508

Url

http://www.ncbi.nlm.nih.gov/pubmed/31178508

MeSH

Adult
Double-Blind Method
Female
Humans
Japan
Male
Medicine, East Asian Traditional/methods*
Middle Aged
Pharyngitis/drug therapy*
Pharyngitis/etiology*
Phytotherapy
Plant Preparations/administration & dosage
Plant Preparations/adverse effects
Plant Preparations/therapeutic use*
Respiratory Tract Infections/complications*
Time Factors

Keywords

kikyo-to; sore throat; upper respiratory tract infection

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KMCRIC
Summary & Commentary

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Korean Study

Abstract

Objective Kikyo-to (KKT) is a fixed combination of glycyrrhiza root and platycodon root extracts. It is an herbal medicine traditionally used in Japan for relieving sore throat associated with acute upper respiratory tract infection (URTI). No controlled studies have yet demonstrated its effect, however. We investigated the efficacy of KKT on sore throat associated with acute URTI. Methods Patients with sore throat who were diagnosed with URTI at the General Medicine Department Office, Akashi Medical Center Hospital, between December 2017 and May 2018 were enrolled. Participants were randomly assigned to two groups at a 1:1 ratio, with stratification by age and sore throat score on a Visual Analogue Scale (VAS), to receive 2.5 g of either KKT or a placebo. Participants and investigators were blinded to group allocation. The primary outcome was the change in sore throat score on VAS 10 minutes after KKT administration. Secondary outcomes were the impact of the sore throat on daily life (none, mild, moderate, and severe) at 10 minutes after administration. Results Thirty-five participants were assigned to each group (n=70, total). The difference in the mean change of sore throat score according to VAS within 10 minutes between the two groups was not statistically significant (KKT 14.40 vs. placebo 17.00; p=0.39). The proportion of patients with a moderate or greater impact of their sore throat on their daily life was also not significantly different between the groups (KKT 22.9% vs. placebo 40.0%; p=0.20). Patients reported no side effects. Conclusion KKT did not significantly relieve sore throat associated with acute URTI compared with placebo.

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