Aortic Aneurysm, Abdominal
Conditions
Keywords
analgesia, TAP-block
Brief summary
The primary outcome of this study was the evaluation of the efficacy of TAP block on pain intensity following open abdominal aortic surgery.
Interventions
DRUGRopivacaine
TAP-block Ropivacaine 0.2% during 48 hours
DRUGPlacebo
TAP-block with placebo
Sponsors
Centre Hospitalier Universitaire Dijon
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Open abdominal aortic surgery (aneurysm or aortobifemoral bypass) * Person who has given his written consent
Exclusion criteria
* Emergency surgery * Patient with infection * Use of opioids in the long term * History of chronic pain * Higher functions incompatible with the functioning of the PCA * Patients under guardianship
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Evaluation of morphine consumption at 24 postoperative hours | 24 hours | Morphine consumption (Patient Controlled Analgesia) statement during the first 24 postoperative hours |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Evaluation of Visual Analogue Scale scores at 24 postoperative hours | 24 hours | Visual Analogue Scale scores statement during the first 24 postoperative hours (minimum pain 0 - maximum pain 10) |
Countries
France
Outcome results
None listed