Cardiovascular and thoracic surgery unit, CHU Dijon
Dijon, 21079, France
NCT Number: NCT03657979
The primary outcome of this study was the evaluation of the efficacy of TAP block on pain intensity following open abdominal aortic surgery.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Dijon, 21079, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
TAP-block Ropivacaine 0.2% during 48 hours
TAP-block with placebo
Time frame: 24 hours
Morphine consumption (Patient Controlled Analgesia) statement during the first 24 postoperative hours
Time frame: 24 hours
Visual Analogue Scale scores statement during the first 24 postoperative hours (minimum pain 0 - maximum pain 10)
Centre Hospitalier Universitaire Dijon
Other
Transversus Abdominis Plane (TAP) Block in Open Abdominal Aortic Surgery : Randomized Controlled Doubled-blind Trial Comparing Ropivacaine 0.2% Versus Placebo
Acronym: TAP-CACAO
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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