Total Intravenous Anaesthesia (TIVA) Versus Spinal Anaesthesia in Patients Undergoing Transurethral Prostate Resection
NCT ID: NCT01118260
Last Updated: 2010-05-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
101 participants
INTERVENTIONAL
2006-01-31
2009-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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TIVA
Total intravenous anaesthesia (TIVA) with propofol and remifentanil
total intravenous anaesthesia
propofol and remifentanil
Spinal
Spinal anaesthesia with bupivacaine and fentanyl
spinal anaesthesia
bupivacaine and fentanyl
Interventions
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total intravenous anaesthesia
propofol and remifentanil
spinal anaesthesia
bupivacaine and fentanyl
Eligibility Criteria
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Inclusion Criteria
* signed informed consent
* elective transurethral prostata resection
Exclusion Criteria
* kidney disease, liver disease
* intolerance against bupivacaine, fentanyl, propofol og remifentanil
* chronic pulmonary disease
* dementia
18 Years
MALE
No
Sponsors
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Asker & Baerum Hospital
OTHER
Responsible Party
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Asker & Baerum Hospital, Vestre Viken HF
Principal Investigators
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Vegard Dahl, MD, PhD
Role: STUDY_CHAIR
Asker & Baerum Hospital
Elisabet Andersson
Role: PRINCIPAL_INVESTIGATOR
Asker & Baerum Hospital
Locations
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Asker & Baerum Hospital
Rud, , Norway
Countries
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Other Identifiers
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2004-002672-42
Identifier Type: -
Identifier Source: org_study_id
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