Clinical Trials Directory

Trials / Completed

CompletedNCT01801124

EXPAREL Infiltrated Into the TAP for Postoperative Analgesia in Unilateral Abdominal Hernia Repair

Evaluation of the Safety and Efficacy of EXPAREL® When Infiltrated Into the Transversus Abdominis Plane (TAP) for Prolonged Postoperative Analgesia in Subjects Undergoing Unilateral Abdominal Hernia Repair

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Pacira Pharmaceuticals, Inc · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Phase 4 study evaluating the effectiveness of EXPAREL when infiltrated into the the Transversus Abdominis Plane (TAP).

Detailed description

This is a prospective, open-label, non-randomized study evaluating the effectiveness of abdominal analgesia when using 266 mg EXPAREL to infiltrate into the TAP unilaterally.

Conditions

Interventions

TypeNameDescription
DRUGEXPARELsingle dose 266 mg of undiluted EXPAREL

Timeline

Start date
2012-04-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2013-02-28
Last updated
2021-03-08
Results posted
2013-09-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01801124. Inclusion in this directory is not an endorsement.