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Clinical Trial Summary

In this study, parturients will be randomized to either internal or external tocodynamometry contractions' follow up. Investigators recruit primiparous, those who try to have vaginal birth after cesarean section and multiparous, who need oxytocin during labor. Primary endpoint is the number of operative labors in each group. Secondary endpoints are the duration of labor, the use of oxytocin and the condition of the newborn.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02941393
Study type Interventional
Source Tampere University Hospital
Contact
Status Completed
Phase N/A
Start date November 2012
Completion date December 31, 2017

See also
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