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Clinical Trial Summary

The purpose of this study is to assess the effectiveness of transversus abdominal plane (TAP) block, thoracic epidural or paravertebral block (PVB) for controlling postoperative pain when compared with opioid you self-administer in your vein using a PCA device. The primary outcome will be postoperative opioid consumption within 24 hours after surgery. A total of 120 subjects will be randomized in a 1:1:1:1 ratio to receive a TAP block, PVB, TEA or no block (PCA alone).Patients in all groups will be cared for using an established enhanced recovery after surgery (ERAS) pathway incorporating a multimodal analgesic regimen using IV acetaminophen and postoperative PCA fentanyl.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Laparoscopic Colorectal Resection

NCT number NCT02164929
Study type Interventional
Source Duke University
Contact
Status Terminated
Phase N/A
Start date December 2013
Completion date March 2015