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Clinical Trial Summary

A multicentre, prospective randomized, active-controlled feasibility trial of volatile-based anaesthesia vs. propofol-based total intravenous anaesthesia to investigate the impact of anaesthesia on long-term (i.e. 5-years) patient cancer outcomes in patients undergoing elective major cancer surgery.


Clinical Trial Description

This study aims to assess the feasibility of conducting a phase IV, multi-centre, single-blinded, randomized control trial (VAPOR-C (Main)). Primary aims To measure the ability to recruit eligible patients into the study. To measure the ability to successfully deliver each of the two anaesthetic techniques (volatile-based general anaesthesia and propofol-based anaesthesia) according to the research protocol. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04074460
Study type Interventional
Source Peter MacCallum Cancer Centre, Australia
Contact
Status Completed
Phase Phase 4
Start date August 27, 2017
Completion date June 30, 2020

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