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Efficacy and Safety of Fospropofol Disodium Versus Propofol for Deep Sedation in Critically Ill Patients

Critical Illness Clinical Trial

Official title:
Efficacy and Safety of Fospropofol Disodium Versus Propofol for Deep Sedation in Critically Ill Patients

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of fospropofol disodium for injection compared to propofol for deep sedation in mechanically ventilated ICU patients.

Clinical Trial Description

This is a randomized, open-label, small sample study using fospropofol disodium and propofol for deep sedation in mechanically ventilated ICU patients. Subjects are randomized to different treatment groups (including 1 for fospropofol disodium and 1 for propofol). Remifentanil is co-administered with fospropofol or propofol. Efficacy and safety profiles of fospropofol disodium and propofol are to be monitoted. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05870514
Study type Interventional
Source Wuhan Union Hospital, China
Contact Xiaobo Yang
Phone 13720311349
Email want.tofly@aliyun.com
Status Recruiting
Phase Phase 2
Start date June 1, 2023
Completion date June 1, 2024
View Details
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