Evidence map›Paper›PMID 42325775›Full record

ArticleAmerican journal of translational research2026

Efficacy and safety of chaishituire granules in influenza treatment: a multi-center, randomized, double-blind, parallel-controlled clinical trial.

Ying Nong, Jiangtao Lin, Guang'en Wang, Hanzhong Xiong, Wei Zhou, Yanhui Liu, Xucheng Li, Shujuan Jiang, Limin Zhao, Yulong Shang and 12 more

Abstract read
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Article in American journal of translational research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

22 authors.

Ying NongDepartment of Pulmonary and Critical Care Medicine, National Clinical Research Center of Respiratory Disease, China-Japan Friendship Hospital Beijing 100029, China.
Jiangtao LinDepartment of Pulmonary and Critical Care Medicine, National Clinical Research Center of Respiratory Disease, China-Japan Friendship Hospital Beijing 100029, China.
Guang'en WangDepartment of Pulmonary Medicine, Handan Hospital of Traditional Chinese Medicine Handan 056000, Hebei, China.
Hanzhong XiongDepartment of Pulmonary and Critical Care Medicine, Ezhou Central Hospital Ezhou 436000, Hubei, China.
Wei ZhouDepartment of Pulmonary and Critical Care Medicine, General Hospital of Ningxia Medical University Yinchuan 750004, Ningxia, China.
Yanhui LiuDepartment of Emergency, Shanxi Fenyang Hospital Fenyang 032200, Shanxi, China.
Xucheng LiDepartment of Emergency, Wuhan Hospital of Traditional Chinese Medicine Wuhan 430014, Hubei, China.
Shujuan JiangDepartment of Pulmonary and Critical Care Medicine, Shandong Provincial Hospital Jinan 250021, Shandong, China.
Limin ZhaoDepartment of Pulmonary and Critical Care Medicine, Henan Provincial People's Hospital Zhengzhou 450003, Henan, China.
Yulong ShangDepartment of Pulmonary Medicine, Xuzhou Cancer Hospital Xuzhou 221005, Jiangsu, China.
Guangbing LuDepartment of Pulmonary and Critical Care Medicine, Meishan Hospital of Traditional Chinese Medicine Meishan 620010, Sichuan, China.
Dapeng ShenDepartment of Internal Medicine, Maternity and Child Health Care of Zaozhuang Zaozhuang 277101, Shandong, China.
Hong ChengDepartment of Emergency, Xiangyang Hospital of Traditional Chinese Medicine Xiangyang 441002, Hubei, China.
Hailong ZhangDepartment of Pulmonary Medicine, First Affiliated Hospital of Henan University of Traditional Chinese Medicine Zhengzhou 450003, Henan, China.
Xuwu SunDepartment of Pulmonary Diseases, Mudanjiang Hospital of Traditional Chinese Medicine Mudanjiang 157000, Heilongjiang, China.
Jun WeiDepartment of Pulmonary Medicine, Tianyou Hospital Affiliated to Wuhan University of Science and Technology Wuhan 430061, Hubei, China.
Zhuohong QinDepartment of Pulmonary Diseases, Changzhi Hospital of Traditional Chinese Medicine Changzhi 046000, Shanxi, China.
Jun WangDepartment of Pulmonary and Critical Care Medicine, Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine Jinan 250001, Shandong, China.
Zengtao SunTianjin Hospital of Traditional Chinese Medicine Tianjin 301600, China.
Lei LiTechnology Center for Drug Research and Evaluation of The China Association of Traditional Chinese Medicine Beijing 100061, China.
Hui ZhenTechnology Center for Drug Research and Evaluation of The China Association of Traditional Chinese Medicine Beijing 100061, China.
Zhuoying FengSinopharm Zhonglian Pharmaceutical Co., Ltd. Wuhan 430000, Hubei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesInformation on the safety and efficacy of chaishituire granules (CSTR) for treating influenza is limited. We evaluated the safety and efficacy of CSTR in shortening the disease and fever course and improving the traditional Chinese medicine (TCM) syndrome score in influenza treatment.

methodsThis multi-center, randomized, positive-drug, parallel-controlled study involved 17 hospitals across China and 221 patients with influenza aged 14-75 years. These patients met the syndrome differentiation criteria for "Wind-Heat Invading the Wei-Exterior". Patients in the CSTR group received CSTR and oseltamivir phosphate dummy capsules, whereas those in the oseltamivir control group received oseltamivir phosphate capsules and CSTR dummy granules. The primary outcomes were the time to complete remission of fever and the main clinical symptoms. The secondary outcomes were the time to elicit antipyretic effects, acetaminophen use, TCM syndrome score, remission rate of main clinical symptoms, single symptom area under the curve (AUC), and the incidence of complications or severe/critical diseases.

resultsThe TCM syndrome score, single symptom AUC, incidence of complications and severe/critical disease, time to complete remission of fever, main clinical symptoms, and initiation of antipyretic effects were evaluated. However, CSTR demonstrated a more rapid action and superior efficacy in alleviating sore throat compared to oseltamivir. The incidence of adverse reactions was similar between the groups.

conclusionsCSTR could be an alternative therapy for influenza virus infections.

Indexed as

Chaishituire granulesefficacyfeverinfluenzaoseltamivir

Identifiers

PMID42325775
PMCPMC13275828

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