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COMPLETED
NCT06261996
NA

Safety and Efficacy of Fospropofol vs Propofol During Invasive Mechanical Ventilation.

Sponsor: Henan Provincial People's Hospital

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to compare the safety and efficacy of fospropofol and propofol during sedation in invasively mechanically ventilated patients in the Anesthesia Intensive Care Unit (AICU). Specific objectives include the following: * Evaluate the sedative effects of fospropofol and propofol in invasively mechanically ventilated patients. Compare the sedative effects of the two medications using relevant clinical indicators and scoring tools, such as the Richmond Agitation-Sedation Scale (RASS). * Compare the safety of fospropofol and propofol during sedation. Monitor medication-related adverse reactions, such as respiratory depression, hypotension, arrhythmias, headache, injection site pain, and assess the differences in adverse reaction incidence between the two medications. * Compare the characteristics of recovery from sedation between PPD and propofol. Focus on the time from sedation to emergence from sedation and compare the differences in recovery time between the two medications. Participants will be sedated with fospropofol or propofol during invasive mechanical ventilation.

Official title: Safety and Efficacy of Fospropofol vs Propofol During Invasive Mechanical Ventilation in Anesthesiology Intensive Care Unit: A Preliminary Study

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2024-04-12

Completion Date

2025-07-10

Last Updated

2026-05-29

Healthy Volunteers

No

Interventions

DRUG

Fospropofol

Fospropofol is administered after admission to the room at a pumping rate of 1 mg/kg/h.

Locations (1)

Henan Provincial People's Hospital

Zhengzhou, China