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Clinical Trial Summary

The purpose of this observational study is to evaluate patients who are planning to administer sugammadex after rocuronium or vecuronium is used. The main questions it aims to answer are: 1. Prescription pattern of sugammadex 2. Effectiveness and safety of sugammadex Since this study is observational, only data generated under daily treatment are to be collected, and no additional tests or drug administration is conducted for the study. The patients are observed from baseline to 24 hours after the initial administration of sugammadex.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05788718
Study type Observational
Source Boryung Pharmaceutical Co., Ltd
Contact MyungSook Hong
Phone +8227088238
Email mshong@boryung.co.kr
Status Recruiting
Phase
Start date April 11, 2023
Completion date August 2025

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