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Clinical Trial Summary

The purpose of this study is to explore the efficacy and safety of ciprofol compared to propofol for non-intubated general anesthesia in patients undergoing transcatheter aortic valve replacement (TAVR).

Clinical Trial Description

This is a study in subjects undergoing transcatheter aortic valve replacement (TAVR). As designed, the study will include 1-day screening period, 1-day observation period, and 1-day safety follow-up. Participants will be randomly assigned to either experimental or control group with a 1:1 allocation, with 12 subjects in each group. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05035069
Study type Interventional
Source Haisco Pharmaceutical Group Co., Ltd.
Contact Fangqiong Li
Phone +86 02867258840
Email [email protected]
Status Not yet recruiting
Phase Phase 4
Start date September 3, 2021
Completion date February 4, 2022

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