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Completed Phase 4 Interventional Results available

Efficacy and Safety of EXPAREL Versus Standard of Care (SoC) in Subjects Undergoing Elective Cesarean Section

ClinicalTrials.gov ID: NCT03853694

Public ClinicalTrials.gov record NCT03853694. 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 Jul 24, 2026, 12:44 AM 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, Active-Controlled Study to Evaluate the Efficacy and Safety of EXPAREL When Administered Via Infiltration Into the Transversus Abdominis Plane Versus Standard of Care in Subjects Undergoing Elective Cesarean Section (CHOICE)

Study identification

NCT ID
NCT03853694
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Pacira Pharmaceuticals, Inc
Industry
Enrollment
167 participants

Conditions and interventions

Interventions

  • 50 mcg Duramorph+ EXPAREL + multi-modal pain regimen Drug
  • 150 mcg Duramorph + multi-modal pain regimen Drug
  • Exparel TAP + multi-modal pain regimen Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Mar 3, 2019
Primary completion
Jan 8, 2020
Completion
Jan 15, 2020
Last update posted
Jul 17, 2022

2019 – 2020

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Stanford University School of Medicine Stanford California 94305
University of Florida- Gainesville Gainesville Florida 32610
University of Florida college of Medicine - Jacksonville Jacksonville Florida 32209
Clinical Research Prime Idaho Falls Idaho 83404
Massachusetts General Hospital Boston Massachusetts 02114
Brigham and Women's Hospital Boston Massachusetts 02115
Henry Ford Hospital Detroit Michigan 48202
Robert Wood Johnson Medical School New Brunswick New Jersey 08901
St. Peter's University Medical Center New Brunswick New Jersey 08901
Columbia University Medical Center/NY Presbyterian Hospital New York New York 10032
Duke University Medical Center Durham North Carolina 27710
Cleveland Clinic Cleveland Ohio 44195
Ohio State University Columbus Ohio 43210
Thomas Jefferson Medical Center Philadelphia Pennsylvania 19107
Magee-Women's Hospital of UPMC Pittsburgh Pennsylvania 15213
The University of Texas Medical Branch Galveston Texas 77555-0877
Inova Health System Falls Church Virginia 22042
West Virginia University Morgantown West Virginia 86506

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 NCT03853694, 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 Jul 17, 2022 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03853694 live on ClinicalTrials.gov.

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