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NCT04290208

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

Status unknown Phase 4 Last updated 28 February 2020
What this trial tests

Phase 4 trial testing Acetaminophen in Postoperative Pain in 130 participants. Status unknown.

Timeline
22 August 2019
Primary endpoint
23 June 2020
23 June 2020

Quick facts

Lead sponsorMain Line Health
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment130
Start date22 August 2019
Primary completion23 June 2020
Estimated completion23 June 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Main Line Health — full company profile →

Who can join

18 and older, female only, with Postoperative Pain or Cesarean Section. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Acetaminophen

Trials testing the same drug.

Other recruiting trials for Postoperative Pain

Currently open trials in the same condition.

Other Main Line Health trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04290208.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing