Ultrasound Guided Caudal Block for Benign Anal Surgery

Status Completed

Clinical Trial Summary

Interventional study that evaluate analgesia and side effects of Ultrasound guided Caudal block preoperatively in benign canal anal surgery

Clinical Trial Description

Postoperative pain is an important symptom in patients after benign anal canal surgery. Caudal block has been described to decrease postoperative pain in this type of surgery. Ultrasound is a tool that facilitates its performance and increases the rate of a successful block.

Objective:

To determine the usefulness of ultrasound guided caudal block in anesthesia and postoperative analgesia in patients scheduled for benign anal surgery. Methods : Interventional study in adult patients that received ultrasound caudal anesthetic block before benign anal surgery. The investigators evaluated analgesic efficacy of this intervention by mean of numeric rating scale ( NRS) for pain after 6, 12 and 24 hours of surgery, rescue analgesia, motor block, urinary retention, surgical conditions and patient satisfaction in postoperative period. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03345511
Study type	Interventional
Source	Universidad de Antioquia
Contact
Status	Completed
Phase	N/A
Start date	November 1, 2015
Completion date	June 30, 2016

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