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Completed Phase 3 Interventional Results available

Opioid Prescription After Cesarean Trial

ClinicalTrials.gov ID: NCT04296396

Public ClinicalTrials.gov record NCT04296396. 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 Sep 9, 2026, 8:08 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

Prescription After Cesarean Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Non-inferiority randomized trial of 5,500 women with a cesarean delivery randomized prior to discharge to either an individualized opioid prescription protocol (IOPP) that includes shared decision making or to a fixed opioid prescription of 20 tablets of oxycodone 5mg.

Study identification

NCT ID
NCT04296396
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
5,521 participants

Conditions and interventions

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
Sep 20, 2020
Primary completion
Apr 6, 2022
Completion
Jul 7, 2022
Last update posted
Oct 2, 2023

2020 – 2022

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
University of Alabama - Birmingham Birmingham Alabama 35233
Northwestern University Chicago Illinois 60611
Columbia University New York New York 10032
University of North Carolina-Chapel Hill Chapel Hill North Carolina 17599
Case Western Reserve-Metrohealth Cleveland Ohio 44109
Ohio State University Columbus Ohio 43210
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104
Magee Womens Hospital of UPMC Pittsburgh Pennsylvania 15213
Brown Univeristy Providence Rhode Island 02905
University of Texas Medical Branch Galveston Texas 77555
University of Texas - Houston Houston Texas 77030
University of Utah Medical Center Salt Lake City Utah 84132

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

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04296396, 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 Oct 2, 2023 · Synced Sep 9, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04296396 live on ClinicalTrials.gov.

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