Calcium Carbonate on Labor Induction

Status Recruiting

Clinical Trial Summary

The investigators aim to evaluate the safety and efficacy of administering calcium carbonate to laboring participants undergoing labor inductions. The investigators hypothesize that calcium carbonate is a low-risk preventative measure to decrease oxytocin induction time and dosage, decrease the rate of labor dystocia, decrease the rate of cesarean deliveries, and demonstrate no differences in maternal or neonatal safety outcomes.

Clinical Trial Description

The investigators plan to assess (1) duration of induction with oxytocin administration, (2) rate of labor dystocia/failed induction, (3) rate of cesarean section, and (4) maternal/neonatal safety. Currently, calcium carbonate is used by clinicians in patients with varying characteristics, at varying doses, and at various times in their labor process based on their professional preference and experience. The investigators will implement a standardized treatment protocol for calcium carbonate use within a defined patient population who voluntarily agree to prospectively receive the intervention and then analyze predetermined safety and efficacy outcomes in comparison to a historical cohort of patients meeting the criteria for the defined patient population who did not have any documented calcium carbonate use during labor. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06352775
Study type	Interventional
Source	Aurora Health Care
Contact	Jessica Kram, MPH
Phone	414-219-5594
Email	jessica.kram@aah.org
Status	Recruiting
Phase	Phase 1
Start date	June 1, 2024
Completion date	December 31, 2025

View Details

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