Evidence map›Paper›PMID 42682357›Full record

ArticleInternational journal of surgery (London, England)2026

A multicenter parallel-group double-blind randomized placebo-controlled phase III clinical trial of generic aprepitant QLG2174 for the prevention of postoperative nausea and vomiting.

Peng Li, Shiyong Li, Wenya Du, Yanjuan Huang, Benfa Zhang, Kai Wang, Zhendong Xu, Yuanhao Qin, Hao Wang, Xia Xu and 27 more

Abstract read
In one paragraph

Article in International journal of surgery (London, England), 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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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

37 authors.

Peng LiDepartment of Anesthesiology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, China.
Shiyong LiDepartment of Anesthesiology and Pain Medicine, Hubei Key Laboratory Of Geriatric Anesthesia and Perioperative Brain Health, and Wuhan Clinical Research, Tongji Hospital, Tongji Medical College, Huazhong University of Science And Technology, Wuhan, China.
Wenya DuDepartment of Anesthesiology, Shandong Provincial Hospital, Jinan, China.
Yanjuan HuangDepartment of Anesthesiology, The Third Affiliated Hospital of Guangxi Medical University, Nanning, China.
Benfa ZhangDepartment of Anesthesiology, Tonghua Central Hospital, Tonghua, China.
Kai WangDepartment of Anesthesiology, People's Hospital of Rizhao, Rizhao, China.
Zhendong XuDepartment of Anesthesiology, Shanghai First Maternity and Infant Hospital, Shanghai, China.
Yuanhao QinDepartment of Anesthesiology, Liuzhou People's Hospital, Liuzhou, China.
Hao WangDepartment of Anesthesiology, Linfen Central Hospital, Linfen, China.
Xia XuDepartment of Anesthesiology, Sanya Central Hospital (Hainan Third People's Hospital), Sanya, China.
Shaoxing LiuDepartment of Anesthesiology, Chengdu Second People's Hospital, Chengdu, China.
Min ZhangDepartment of Anesthesiology, Suining Central Hospital, Suining, China.
Tiantian ZouDepartment of Anesthesiology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Wei GaoDepartment of Anesthesiology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Foquan LuoCenter for Rehabilitation Medicine, Department of Anesthesiology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, China.
Zhonghua ChenDepartment of Anesthesiology, Shaoxing People's Hospital, Shaoxing, China.
Furong HuangAnesthesia and Surgery Department, Changde First People's Hospital, Changde, China.
Chun MaDepartment of Anesthesiology, Chongqing University Affiliated Fuling Hospital, Chongqing, China.
Chunling WangDepartment of Anesthesiology, Center for Rehabilitation Medicine, Qilu Hospital of Shandong University, Jinan, China.
Shu'An JinDepartment of Anesthesiology, Center for Rehabilitation Medicine, Central Hospital Affiliated to Shandong First Medical University, Jinan, China.
Chun ChenDepartment of Anesthesiology, Yichang Central People's Hospital, Yichang, China.
Jun JingDepartment of Anesthesiology, People's Hospital of Maanshan, Maanshan, China.
Ling ZhaoDepartment of Anesthesiology, The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.
Junqing LiDepartment of Anesthesiology, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Huiyu LuoDepartment of Anesthesiology, Xiangyang First People's Hospital, Xiangyang, China.
Changming YangAnesthesia and Surgery Department, Jingmen Central Hospital, Jingmen, China.
Chan WangAnesthesia and Surgery Department, Jingmen Central Hospital, Jingmen, China.
Yanzhuo ZhangDepartment of Anesthesiology, Liuzhou Worker's Hospital, Liuzhou, China.
Xiaoling HuAnesthesia and Surgery Department, The First Affiliated Hospital of University of South China, Hengyang, China.
Yalan LiDepartment of Anesthesiology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Xiaoyi NingClinical Research and Development Centre, Qilu Pharmaceutical, Jinan, China.
Yang YanClinical Research and Development Centre, Qilu Pharmaceutical, Jinan, China.
Yunfei JuClinical Research and Development Centre, Qilu Pharmaceutical, Jinan, China.
Juan WangClinical Research and Development Centre, Qilu Pharmaceutical, Jinan, China.
Mengchang YangDepartment of Anesthesiology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, China.
Yuelan WangDepartment of Anesthesiology, Shandong Provincial Hospital, Jinan, China.
Ailin LuoDepartment of Anesthesiology and Pain Medicine, Hubei Key Laboratory Of Geriatric Anesthesia and Perioperative Brain Health, and Wuhan Clinical Research, Tongji Hospital, Tongji Medical College, Huazhong University of Science And Technology, Wuhan, China.ORCID https://orcid.org/0000-0001-8826-5588

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Postoperative nausea and vomiting (PONV), a common gastrointestinal disorder following surgery, primarily occurs within 6-24 hours postoperatively, with an incidence rate of approximately 30% in general surgical patients. QLG2174 (generic aprepitant) is a neurokinin-1 (NK-1) receptor antagonist exerting antiemetic effects by blocking the binding of substance P to NK-1 receptors. This study aimed to evaluate the efficacy and safety of QLG2174 for preventing PONV in Chinese patients. Materials and methods: This was a multi-center, parallel-group, double-blind, randomized, placebo-controlled, phase 3 clinical trial. Patients with ≥2 PONV risk factors and scheduled for elective laparoscopic gynecologic or abdominal surgery under general anesthesia were randomized 1:1 to receive either QLG2174 32 mg or placebo via intravenous injection within 30 seconds before anesthesia induction. The primary efficacy endpoint was the proportion of patients achieving complete response (CR, defined as no vomiting and no rescue therapy use) within 24 hours postoperatively. Results: A total of 515 patients were enrolled. The CR rate within 24 hours postoperatively was significantly higher in the QLG2174 group compared with that in the placebo group [70.7% (181/256) versus 44.0% (114/259); adjusted rate difference 26.6% (95% confidence interval, 18.4-34.7), Conclusion: QLG2174 significantly increased CR rate compared with placebo and demonstrated promising efficacy in preventing PONV in patients scheduled for elective laparoscopic surgery under general anesthesia.

Indexed as

aprepitantgynecologic surgical procedureslaparoscopyNK-1 receptor antagonistpostoperative nausea and vomiting

Identifiers

PMID42682357
PMCPMC13336602

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.