Clinical trialNCT06550089WithdrawnPhase 2Interventional

High Or Low Dose pOstpartUm Oxytocin at the Time of Cesarean Birth

SponsorUniversity of ChicagoEnrollment0Cesarean Section ComplicationsPostpartum HemorrhagePregnancy Complications

View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This is a study to investigate whether it is feasible to conduct a randomized controlled trial (RCT) of a high dose of oxytocin versus the standard low-dose oxytocin. Further the investigators, aim to assess whether there are differences in health outcomes between both arms of the study.

clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

Anna Palatnik, MD
Medical College of Wisconsin
Principal Investigator
clinicaltrials.gov ↗
Ashish Premkumar, MD, PhD
University of Chicago
Principal Investigator
clinicaltrials.gov ↗

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

No facility list is in our current data snapshot for this study. The registry record on ClinicalTrials.gov ↗ carries any published locations. Why? →

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Oxytocin

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start: 31 Oct 2024
Primary completion: 31 Oct 2026
Completion: 31 Dec 2026
Last update posted: 10 Dec 2024
Registered enrollment: 0
Registry id: NCT06550089

clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.