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Spots Global Cancer Trial Database for Volatile Anaesthesia and Perioperative Outcomes Related to Cancer: The VAPOR-C Trial

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Trial Identification

Brief Title: Volatile Anaesthesia and Perioperative Outcomes Related to Cancer: The VAPOR-C Trial

Official Title: Volatile Anaesthesia and Perioperative Outcomes Related to Cancer: The VAPOR-C Trial

Study ID: NCT04316013

Study Description

Brief Summary: VAPOR-C is a randomised study of the impact of IV versus inhaled anaesthesia (propofol versus sevoflurane) and lidocaine versus no lidocaine on duration of disease free survival inpatients with either colorectal or non small cell lung cancer.

Detailed Description: VAPOR-C is a pragmatic, event-driven, randomised controlled trial, with a single blind 2x2 factorial design for sevoflurane/propofol and for intravenous lidocaine infusion / no lidocaine infusion. This trial is designed to test for superiority in disease free survival (DFS) of propofol (total intravenous anaesthesia -TIVA) over sevoflurane (inhalational volatile anaesthesia) and intravenous lidocaine over no lidocaine in patients undergoing surgery for colorectal or non small cell lung cancer (NSCLC). The combination of two cancer types will help address the need to demonstrate the effects of anaesthetic technique across cancers to inform generalisable anaesthesia guidelines. Both NSCLC and colorectal cancer are important for this study due to high incidence rate, many longer-term survivors, and importantly the high risk of local or distant recurrence despite complete surgical resection. In addition, the study will collect additional data in a nested cohort related to the exploratory objectives. The study aims to recruit 3,500 patients in Australia, New Zealand, Canada, United States and Europe.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Cleveland Clinic, Cleveland, Ohio, United States

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

The University of Texas MD Anderson Cancer Centre, Houston, Texas, United States

Chris O'Brien Lifehouse, Camperdown, New South Wales, Australia

Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia

Prince of Wales Hospital, Randwick, New South Wales, Australia

Royal Brisbane and Women's Hospital, Herston, Queensland, Australia

Mackay Base Hospital, Mackay, Queensland, Australia

RedCliffe Hospital, Redcliffe, Queensland, Australia

Rockhampton Hospital, Rockhampton, Queensland, Australia

Gold Coast University Hospital, Southport, Queensland, Australia

Princess Alexandra Hospital, Woolloongabba, Queensland, Australia

Royal Adelaide Hospital, Adelaide, South Australia, Australia

Royal Hobart Hospital, Hobart, Tasmania, Australia

Ballarat Base Hospital, Ballarat Central, Victoria, Australia

Box Hill Hospital, Box Hill, Victoria, Australia

Northern Hospital, Epping, Victoria, Australia

St Vincent's Hospital, Melbourne, Fitzroy, Victoria, Australia

Western Health Footscray Hospital, Footscray, Victoria, Australia

Austin Health, Heidelberg, Victoria, Australia

Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia

The Alfred Hospital, Melbourne, Victoria, Australia

The Royal Melbourne Hospital, Parkville, Victoria, Australia

Goulburn Valley Health, Shepparton, Victoria, Australia

Northeast Health, Wangaratta, Wangaratta, Victoria, Australia

North Shore Hospital, Auckland, , New Zealand

Auckland City Hospital, Auckland, , New Zealand

Contact Details

Name: Bernhard Riedel, MB.ChB

Affiliation: Peter MacCallum Cancer Centre, Australia

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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