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Trials / Terminated

TerminatedNCT02908126

Compare Efficacy of Oxytocin Administrations on Postpartum Uterine Contractility

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
4 (actual)
Sponsor
Oxytone Bioscience BV · Industry
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

This is a Phase I open-label, parallel-group clinical study in healthy term pregnant females undergoing a caesarean section. Two administrations of oxytocin will be tested, after which uterine contractility will be assessed.

Conditions

Interventions

TypeNameDescription
DRUGOxytocinOxytocin drug

Timeline

Start date
2018-04-03
Primary completion
2019-06-27
Completion
2019-06-27
First posted
2016-09-20
Last updated
2019-11-22

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT02908126. Inclusion in this directory is not an endorsement.

Compare Efficacy of Oxytocin Administrations on Postpartum Uterine Contractility (NCT02908126) · Clinical Trials Directory