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A Comparison of IV Versus PO Acetaminophen Postoperatively for Opioid Consumption After Cesarean Section

NCT04290208 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2020-02-28

No results posted yet for this study

Summary

This randomized controlled study will compare narcotic consumption between two groups: patients that receive a perioperative dose of IV acetaminophen versus patients that receive a perioperative dose of oral liquid acetaminophen for scheduled cesarean section.

Conditions

Interventions

DRUG

Acetaminophen

IV Acetaminophen

DRUG

Acetaminophen

Acetaminophen liquid syrup

DRUG

Placebos

Flavored, non-medicated (placebo) liquid syrup

DRUG

Placebos

IV salt solution (non-medicated)

Sponsors & Collaborators

  • Sharpe-Strumia Research Foundation

    collaborator OTHER

  • Main Line Health

    lead OTHER

Principal Investigators

  • Dmitri Chamchad, MD · Main Line Health

  • Robert Day, MD · Bryn Mawr Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-22
Primary Completion
2020-06-23
Completion
2020-06-23
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04290208 on ClinicalTrials.gov