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Completed Phase 3 Interventional

Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery

ClinicalTrials.gov ID: NCT02959476

Public ClinicalTrials.gov record NCT02959476. 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 Jun 26, 2026, 10:10 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 Double Blind, Multi-center, Randomized, Placebo-Controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Ropivacaine 0.2% Pre-Filled Dispenser for the Treatment of Postsurgical Pain in Patients Undergoing Cesarean Delivery

Study identification

NCT ID
NCT02959476
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
BioQ Pharma, Inc.
Industry
Enrollment
132 participants

Conditions and interventions

Interventions

  • Ropivacaine Drug
  • Placebos Drug

Drug

Eligibility (public fields only)

Age range
Not listed
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 12, 2017
Primary completion
Aug 9, 2018
Completion
Aug 9, 2018
Last update posted
Aug 13, 2018

2017 – 2018

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
Clinical Research Associates, Inc. Birmingham Alabama 35205
Shoals Medical Trials, Inc. Sheffield Alabama 35660
University of California, Irvine Orange California 92868
Vision Clinical Research Wellington Florida 33414
Clinical Research Prime Idaho Falls Idaho 83404
MedPharmics, LLC Biloxi Mississippi 39531
Duke University Medical Center Durham North Carolina 27606
Compass Clinical Trial Beaumont Texas 77702
Physician's Research Options, LLC- Corner Canyon OB/GYN Draper Utah 84020
Health Sciences Center- University of Utah Salt Lake City Utah 84112
West Virginia University Morgantown West Virginia 26506

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 NCT02959476, 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 Aug 13, 2018 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02959476 live on ClinicalTrials.gov.

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