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Clinical Trial Summary

To evaluate the feasibility of a pragmatic, large scale, comparative effectiveness, randomized evaluation of patient experience of intravenous propofol versus inhaled volatile anesthesia.


Clinical Trial Description

Two-center single-blinded randomized feasibility study, with randomization 1:1 to either propofol TIVA or inhaled volatile general anesthesia for patients who are receiving elective non-cardiac surgery. Patients will be stratified by clinical site with 150 participants per site. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05346588
Study type Interventional
Source Washington University School of Medicine
Contact
Status Completed
Phase Phase 3
Start date September 29, 2022
Completion date June 28, 2023

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