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Clinical Trial Summary

This double-blind, randomized controlled trial will evaluate the effect of the route of administration of 10 IU of oxytocin on the average blood loss postpartum. Participants will be randomized to receive 10 IU of oxytocin by IV infusion or 10 IU of oxytocin by injection IM


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02954068
Study type Interventional
Source Gynuity Health Projects
Contact
Status Completed
Phase Phase 4
Start date December 1, 2016
Completion date October 1, 2017

See also
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