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Acute Post-operative Pain in Colon Resections — ERAS-PO  

Analgesia Clinical Trial

Official title:
Treatment of Acute Post-operative Pain in Patients Undergoing Laparoscopic Colon Resections

Clinical Trial Summary

Objective of the study is to compare three different analgesic techniques in patients undergoing laparoscopic colon resections: peridural catheter, patient controlled analgesia of endovenous morphine and patient controlled analgesia of sufentanil sublingual tablets.

Clinical Trial Description

159 patients undergoing laparoscopic colon resections will be enrolled and randomized in three different groups.

Patients in the first group will be subjected to the positioning of a peridural catheter with a continuous infusion of ropivacaine 0,2%99 ml+sufentanil 50 mcg at an infusion rate of 4-6 ml/h.

In the second group participants will receive an intraoperative bolus of morphine (0,05mg/kg) and post-operatively a patient controlled analgesia of endovenous morphine (injection dose 1 mg,lock-out 10 minutes,maximum morphine dosage for hour 4 mg).

In the third group the investigators will adopt an intraoperative bouls of morphine (0,05mg/kg) and post-operatively a patient controlled analgesia of sufentanil sublingual tablets( 15 mcg, lock-out 20 minutes) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03403842
Study type Interventional
Source IRCCS San Raffaele
Contact stefano turi, md
Phone 0226432656
Email turi.stefano@hsr.it
Status Recruiting
Phase N/A
Start date February 1, 2018
Completion date August 1, 2019
View Details
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