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Clinical Trial Summary

Exploring the 90% effective dose (ED90) of fospropofol disodium in induction and maintenance of anesthesia in adults of different ages, providing more clinical evidence for the application of fospropofol disodium in clinical anesthesia


Clinical Trial Description

As a newly marketed sedative hypnotic agent, fospropofol disodium is currently the only water-soluble precursor drug of propofol in China. It has the characteristics of long duration of action, low incidence of injection pain, respiratory and circulatory system related adverse events, and no lipid metabolism related adverse reactions, providing anesthesiologists with another sedative option during surgery. However, there are currently few clinical observation studies on this drug, and there have been no reports on its effective dosage in different age groups. Therefore, this study aims to observe the 90% effective dose (ED90) in anesthesia induction and maintenance in adults of different ages, providing effective clinical evidence for its application in clinical anesthesia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06344325
Study type Interventional
Source Tongji Hospital
Contact mujun Chang, Dr.
Phone +862783663625
Email changmujun@hotmail.com
Status Not yet recruiting
Phase Phase 4
Start date May 1, 2024
Completion date March 31, 2026

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