Comparison of Postoperative Anti-nausea and Vomiting Effect Between Glycopyrronium and Ondansetron

NCT05265507 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 480

Last updated 2023-02-24

No results posted yet for this study

Summary

To compare the anti-nausea and vomiting effect between glycopyrronium and ondansetron for patients receiving elective surgery under general anesthesia. Based on this study the investigators intend to explore the feasibility of using glycopyrronium to prevent postoperative nausea and vomiting.

Conditions

  • Postoperative Nausea and Vomiting

Interventions

DRUG

Glycopyrronium

Glycopyrronium (0.2mg) was intravenously given at the ending of the surgery.

DRUG

Ondansetron

Glycopyrronium (4mg) was intravenously given at the ending of the surgery.

Sponsors & Collaborators

  • Chongqing University Jiangjin Hospital

    collaborator UNKNOWN
  • Chongqing Medical University

    collaborator OTHER
  • The People's Hospital of DAZU ,Chongqing

    collaborator UNKNOWN
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • The People's Hospital of Tongliang District, Chongqing city

    collaborator UNKNOWN
  • Chongqing Medical Center for Women and Children

    collaborator OTHER
  • Dianjiang People's Hospital of Chongqing

    collaborator UNKNOWN
  • The Ninth People's Hospital of Chongqing

    collaborator UNKNOWN
  • The People's Hospital of Yubei District of Chongqing city

    collaborator UNKNOWN
  • Chongqing Yongchuan District People's Hospital

    collaborator UNKNOWN
  • The First People's Hospital Of Chongqing Liang Jiang New Area

    collaborator UNKNOWN
  • ChongGang General Hospital

    collaborator UNKNOWN
  • The People's Hospital of Nanchuan

    collaborator UNKNOWN
  • People's Hospital of Pengshui County

    collaborator UNKNOWN
  • Yunyang people's Hospital

    collaborator UNKNOWN
  • Chongqing Liangping District People's Hospital

    collaborator UNKNOWN
  • Jiulongpo People's Hospital of chongqing

    collaborator UNKNOWN
  • The People's Hospital of Qijiang District,Chongqing

    collaborator UNKNOWN
  • University-Town Hospital of Chongqing Medical University

    collaborator OTHER
  • Chongqing Public Health Medical Center

    collaborator OTHER
  • CHONGQING BANAN HOSPITAL OF TCM

    collaborator UNKNOWN
  • The Second Affiliated Hospital of Chongqing Medical University

    lead OTHER

Principal Investigators

  • He Huang, MD · The Second Affiliated Hospital, Chongqing Medical University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-21
Primary Completion
2023-05-30
Completion
2023-05-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05265507 on ClinicalTrials.gov