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ISRCTN
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ISRCTN32814070
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ClinicalTrials.gov identifier
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Public title
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Does the route of administration of ketamine influence perioperative and postoperative analgesia?
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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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N0084113941
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Study hypothesis
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To compare the duration of analgesia with ketamine given by two different routes.
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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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Signs and Symptoms: Pain
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Participants - inclusion criteria
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Children undergoing herniotomy, orchidoplexy and repair of hydrocoele.
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Participants - exclusion criteria
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Not provided at time of registration
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Anticipated start date
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28/06/2002
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Anticipated end date
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01/06/2004
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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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Three groups, 64 in each group, with a total of 192.
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Interventions
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1. Caudal ketamine
2. Intravenous ketamine
3. No ketamine
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Primary outcome measure(s)
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1. Duration of postoperative analgesia
2. Nausea, sedation and motor blockade
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Secondary outcome measure(s)
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Not provided at time of registration
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Sources of funding
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The North and South Bank Research and Development Consortium (UK)
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Trial website
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Publications
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Contact name
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Dr
Reshma
Goorah
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Address
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Department of Anaesthetics
Hull Royal Infirmary
Anlaby Road
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City/town
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Hull
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Zip/Postcode
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HU3 2JZ
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Country
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United Kingdom
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Email
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Sponsor
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Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
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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 (0)20 7307 2623
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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.doh.gov.uk
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Date applied
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12/09/2003
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Last edited
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18/12/2008
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Date ISRCTN assigned
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12/09/2003
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