The main objectives of the trial are the efficacy and safety of intercostal nerve block in the midaxillary line versus paravertebral block, both guided by ultrasound in patients scheduled for not reconstructive breast surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
120
Hospital Abente y Lago. Complejo Hospitalario Universitario A Coruña
A Coruña, Spain
RECRUITINGpain score: verbal simple scale
admission to post-anesthesia care unit (PACU)
Time frame: 0,3,6,12,18 and 24h
pain score: visual number scale
post-admission to PACU
Time frame: 0, 3, 6,12, 18, 24h
opioid requirements
0 dose/ 1 dose/ 2 or more doses
Time frame: 24 h
sleep quality
bad/regular/good
Time frame: 24 h
amount of sleep
\< 3h/ 3-6h, \>6h
Time frame: 24 h
percentage of participants with nausea and vomiting
without symptoms/ nausea/vomiting/ both symptoms
Time frame: 24 hours
Number of Participants with Serious and Non-Serious Adverse Events
directly due to block nerve and general complications
Time frame: 24 h
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