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Completed Phase 4 Interventional Accepts healthy volunteers Results available

Evaluate the Safety and Efficacy of EXPAREL When Administered Via Infiltration Into the TAP vs. Bupivacaine Alone in Subjects Undergoing Elective C-Sections

ClinicalTrials.gov ID: NCT03176459

Public ClinicalTrials.gov record NCT03176459. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 27, 2026, 6:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Active-controlled Study to Evaluate the Safety and Efficacy of EXPAREL When Administered Via Infiltration Into the Transversus Abdominis Plane (TAP) Versus Bupivacaine Alone in Subjects Undergoing Elective Cesarean Section

Study identification

NCT ID
NCT03176459
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Pacira Pharmaceuticals, Inc
Industry
Enrollment
186 participants

Conditions and interventions

Interventions

  • Bupivacaine Drug
  • Exparel + Bupivacaine Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2017
Primary completion
Nov 19, 2018
Completion
Dec 3, 2018
Last update posted
Jan 5, 2021

2017 – 2018

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Loma Linda University Loma Linda California 92354
Stanford University Medical Center Stanford California 94305
Massachusetts General Hospital Boston Massachusetts 02114
Brigham and Women's Hospital Boston Massachusetts 02115
Henry Ford Health Systems Detroit Michigan 48202
University of Minnesota Minneapolis Minnesota 55455
St. Peter's University Medical Center New Brunswick New Jersey 08901
Columbia Universtiy Medical Center New York New York 10032
Duke Regional Hospital Durham North Carolina 27704
Duke University Medical Center Durham North Carolina 27710
Inova Fairfax Medical Center Falls Church Virginia 22042
West Virginia University School of Medicine Morgantown West Virginia 26505

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03176459, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 5, 2021 · Synced Apr 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03176459 live on ClinicalTrials.gov.

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