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ISRCTN
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ISRCTN90337900
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ClinicalTrials.gov identifier
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Public title
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BIS monitoring and depth anaesthesia for cardioversion
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Scientific title
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Acronym
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N/A
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Serial number at source
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N0019186908
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Study hypothesis
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To compare differences in the haemodynamic parameters during cardioversion with sevoflurane and propofol anaesthesia.
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Ethics approval
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Not provided at time of registration
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Study design
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Randomised controlled trial
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Countries of recruitment
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United Kingdom
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Disease/condition/study domain
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Surgery: Anaesthesia
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Participants - inclusion criteria
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Patients undergoing elective day case cardioversions for cardiac arrhythmias
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Participants - exclusion criteria
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Any patient not willing to consent or not able to consent, with history of malignant hyperthermia or hypersensitivity to propofol.
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Anticipated start date
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08/11/2006
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Anticipated end date
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01/06/2007
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Status of trial
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Completed
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Patient information material
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Target number of participants
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60
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Interventions
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BIS monitoring vs standard treatment
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Primary outcome measure(s)
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Optimisation of depth of anaesthesia.
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Secondary outcome measure(s)
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To assess appropriateness of using BIS monitor when anaesthetising patients for cardioversion.
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Sources of funding
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East Sussex Hospitals NHS Trust
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Trial website
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Publications
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Contact name
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Dr
M
Parsloe
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Address
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Department of Anaesthesia
Conquest Hospital
The Ridge
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City/town
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St Leonards on Sea
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Zip/Postcode
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TN37 7RD
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Country
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United Kingdom
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Sponsor
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Record Provided by the NHSTCT Register - 2007 Update - Department of Health
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Address
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The Department of Health, Richmond House, 79 Whitehall
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City/town
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London
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Zip/Postcode
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SW1A 2NL
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Country
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United Kingdom
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Tel
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+44 (0)20 7307 2622
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Fax
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+44
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Email
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dhmail@doh.gsi.org.uk
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Sponsor website:
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http://www.dh.gov.uk/Home/fs/en
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Date applied
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28/09/2007
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Last edited
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06/11/2007
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Date ISRCTN assigned
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28/09/2007
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