Laparoscopic Cholecystectomy Clinical Trial
Official title:
Double Blind Randomized Phase III Controlled Trial Comparing the Effect of Intraperitoneal Nebulization of Ropivacaine With Intraperitoneal Instillation of Ropivacaine on Pain Control After Laparoscopic Cholecystectomy
Studies evaluating intraperitoneal local anesthetic instillation for pain relief after laparoscopic procedures have provided conflicting results. This randomized, double-blind study was designed to assess the effects of a novel intraperitoneal local anesthetic administration technique using nebulization on pain relief after laparoscopic cholecystectomy.
Studies evaluating intraperitoneal local anesthetic (LA) instillation for pain relief after
laparoscopic cholecystectomy have provided conflicting results. One of the factors that
might contribute to failure of the instillation technique may be related to inadequate
distribution of local anesthetic throughout the peritoneal surface. In contrast,
nebulization should provide a uniform spread of drugs throughout the peritoneal cavity and
thus may be beneficial to improve pain relief after laparoscopic procedures. A recent study
reported that bupivacaine nebulization significantly reduced pain after laparoscopic
cholecystectomy compared with bupivacaine instillation in the gallbladder bed. However,
these investigators used a custom-made nebulization system that needs a separate gas source
and tubing that is cumbersome and may not be easily available.
Recently, the investigators reported that a microvibration-based nebulization device
(Aeroneb Pro® system, Aerogen, Galway, Ireland) could be used for ropivacaine delivery into
the insufflation gas required to create pneumorpeitoneum. The investigators hypothesized
that intraperitoneal ropivacaine nebulization would provide superior pain relief after
laparoscopic cholecystectomy than intraperitoneal ropivacaine instillation. This randomized,
double blind, controlled clinical trial was designed to assess the analgesic efficacy of
ropivacaine nebulization using the Aeroneb Pro® device laparoscopic cholecystectomy compared
with intraperitoneal ropivacaine instillation.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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