Clinical Trials Directory

Trials / Completed

CompletedNCT03345511

Ultrasound Guided Caudal Block for Benign Anal Surgery

Ultrasound Guided Analgesic Caudal Block in Anal Canal Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
23 (actual)
Sponsor
Universidad de Antioquia · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREUltrasound Guided Caudal BlockUsing an external ultrasound probe, the investigators guided a 18 gauge epidural needle into the caudal space and injected a local anesthetic solution consisting in bupivacaine 0.25%, lidocaine 1% and dexamethasone 8mg in the caudal space.

Timeline

Start date
2015-11-01
Primary completion
2016-05-30
Completion
2016-06-30
First posted
2017-11-17
Last updated
2018-04-30

Locations

1 site across 1 country: Colombia

Source: ClinicalTrials.gov record NCT03345511. Inclusion in this directory is not an endorsement.