drugset / Trial / NCT06573489

Efficacy and Safety of Fospropofol in Adult Laparoscopic Surgery: A Clinical Trial

NCT06573489

Phase 4 Recruiting 373 enrolled Hui Xu
RandomizedSingle-groupDouble-blindTreatment

Summary

This protocol is a clinical study of fospropofol disodium for general anesthesia in adults undergoing laparoscope-assisted abdominal surgery. The study has three main objectives: First, to explore the use of propofol disodium as the lowest effective dose for induction of general anesthesia; Secondly, to evaluate the efficacy and safety of fospropofol disodium in the maintenance phase of general anesthesia, and to determine its effective dose range; Finally, the effects of fospropofol disodium on Bispectral Index during induction, maintenance and recovery were studied, and compared with propofol to understand its characteristic changes. The randomized, single-blind, controlled design of the study, with an expected enrollment of 373 patients, was designed to achieve its objectives through a three-phase trial design to provide important clinical information about the safety and efficacy of the use of propofol disodium.

Timeline

Start
2024-09-15
Primary completion
2025-10-01
Completion
2026-07-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Propofol Small molecule
Subject fospropofol Small molecule

Indications

No indication recorded.