Clinical Trials Directory

Trials / Completed

CompletedNCT01501565

Analgesic Efficacy of Ultrasound-guided Transverse-abdominal Plain Blockade in Urological Surgery

Ultrasound-guided Analgesic Transverse Abdominal Plain Blockade in the Multimodal Pain Management for Laparoscopic Urological Surgery. Analgesic Efficacy Assessment.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
141 (actual)
Sponsor
Fundacio Puigvert · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare pain level (according to numerical score)at 4, 8, 12 and 24 postoperative hours between patients under transverse abdominal plain blockade (TAP) and patients under conventional analgesia. Also the opioid consumption is assessed.

Conditions

Interventions

TypeNameDescription
PROCEDUREPostoperative transverse abdominal plain (TAP) blockadeBupivacaine 0.25%. Maximum 150 mg. A maximum of 75 mg bupivacaine is administered in each side (posterior and subcostal TAP) in a single puncture.

Timeline

Start date
2011-12-01
Primary completion
2012-11-01
Completion
2012-11-01
First posted
2011-12-29
Last updated
2012-11-16

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT01501565. Inclusion in this directory is not an endorsement.