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Spots Global Cancer Trial Database for Volatile Anaesthesia and Perioperative Outcomes Related to Cancer Feasibility Study

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Trial Identification

Brief Title: Volatile Anaesthesia and Perioperative Outcomes Related to Cancer Feasibility Study

Official Title: Volatile Anaesthesia and Perioperative Outcomes Related to Cancer (VAPOR-C): A Feasibility Study

Study ID: NCT04074460

Study Description

Brief 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.

Detailed 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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Peter MacCallum Cancer Centre, Melbourne, , Australia

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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