Prophylactic Intravenous Calcium Gluconate to Decrease Blood Loss at Time of Cesarean Delivery in Pregnant Patients at High Risk for Uterine Atony

Recruiting Phase 2 Interventional Study
Blood Loss, Surgical Blood Loss, Postoperative Uterine Atony
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Female
Trial phase
Phase 2
Study type
Interventional
Purpose
Prevention
Participants needed
140 (estimated)
Sponsor
University of Michigan · Other
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About This Trial

This research study is being done to learn what effect a single dose of calcium gluconate will have on blood loss at the time of cesarean delivery in pregnancy patients at high risk for uterine atony.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * English speaking * Viable Intrauterine Pregnancy, Gestational Age ≥24 weeks * Labor Converted to Cesarean Delivery at High Risk for Atonic Bleeding Defined as: Any exposure to oxytocin infusion for labor augmentation or induction prior to cesarean delivery * Or Scheduled Cesar…
Contacts

AnneMarie Opipari, MD

734-763-8048

opipari@med.umich.edu

CONTACT

Hero Eisley

734-763-8048

parkerdh@umich.edu

CONTACT