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Pharmacokinetics of Oral Calcium Carbonate in Parturients
Sponsor: Stanford University
Summary
This study investigates the time course of change in calcium in the blood after a pregnant subject takes an oral dose of calcium carbonate (commonly marketed as "Tums"). This information is important for trials investigating whether calcium can reduce postpartum hemorrhage, bleeding after delivery.
Key Details
Gender
FEMALE
Age Range
18 Years - 45 Years
Study Type
INTERVENTIONAL
Enrollment
60
Start Date
2025-01
Completion Date
2025-10
Last Updated
2024-11-20
Healthy Volunteers
No
Interventions
Oral calcium carbonate
All participants receive a single, open-label dose of oral calcium carbonate 3000mg
Locations (1)
Stanford Children's Health, Lucile Packard Children's Hospital
Stanford, California, United States