A Study to Compare Two Techniques for Pain Control After Bariatric Surgery
Pain, Postoperative, Bariatric Surgery Candidate
About this trial
This is an interventional treatment trial for Pain, Postoperative focused on measuring Transversus Abdominis Plane (TAP) Block, Local Anesthetic Infiltrations
Eligibility Criteria
Inclusion Criteria:
- patients undergoing elective bariatric surgery
- age ≥ 18 years
- signed informed consent
Exclusion Criteria:
- Pregnant or lactating women,
- known allergy to local anesthetics
- Chronic pain syndrome.
Sites / Locations
- Ospedale Regionale di Lugano, Civico e Italiano
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Arm A - laparoscopic assisted TAP block
Arm B - PSI
Patients will undergo the planned bariatric intervention according to the standard of treatment. A solution of 20 ml of the local anesthetic Ropivacaine (0.25%) is then injected for postoperative pain control according to the allocated procedure (TPA).
Patients will undergo the planned bariatric intervention according to the standard of treatment. A solution of 20 ml of the local anesthetic Ropivacaine (0.25%) is then injected for postoperative pain control according to the allocated procedure (PSI).