Ultrasound Guided Transversus Abdominis Plane Block With Ropivacaine vs Placebo for Abdominal Hysterectomy: a Double-blinded, Randomized Clinical Trial
NCT ID: NCT01743378
Last Updated: 2013-08-30
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
NA
48 participants
INTERVENTIONAL
2011-02-28
2013-06-30
Brief Summary
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Two groups of each 24 patients. All patients are given general anesthesia. The patients are randomized to have a ultrasound guided bilateral transversus abdominis plane block with either 2 x 20 ml 0,75 % ropivacaine or 2 x 20 ml of 0,9 saline. All patients are provided with a PCA for self administration of morphine.
Pain score on visual analog scale, nausea and vomiting are monitored at 1, 2, 4, 6, 8 and 24 hours postoperatively as well as the total consumption of morphine after 24 hours.
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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TAP Block Ropivacaine 0,75 %
Bilateral Transversus Abdominis Plane Block with 2 x 20 ml Ropivacaine 0,75 %
TAP Block Ropivacaine 0,75 %
TAP Block Saline 0,9 %
Bilateral Transversus abdominis plane block with 2 x 20 ml Saline 0,9 %
TAP Block Saline 0,9 %
Interventions
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TAP Block Ropivacaine 0,75 %
TAP Block Saline 0,9 %
Eligibility Criteria
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Inclusion Criteria
* Must be able to understand and speak danish
* Must be able to give verbal and written consent
Exclusion Criteria
* Daily treatment with opoids or glucocorticoids
* Allergy towards any kind of localanesthetic drug
* Intolerance toward morphine
* Psychiatric desease
* Age below 18
18 Years
FEMALE
No
Sponsors
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Hvidovre University Hospital
OTHER
Responsible Party
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Billy B Kristensen
MD
Locations
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Hvidovre Hospital
Hvidovre, Capital Region, Denmark
Countries
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Other Identifiers
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H-1-2010-068
Identifier Type: -
Identifier Source: org_study_id