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Delivery Timing in Morbidly Adherent Placentas: a Randomized, Controlled Trial — MAP  

Placenta Accreta Clinical Trial

Clinical Trial Summary

This is a randomized controlled trial to investigate the optimal timing of delivery in clinically stable women with a suspected morbidly adherent placenta.

Clinical Trial Description

This is a randomized controlled trial to investigate the optimal timing of delivery in clinically stable women with a suspected morbidly adherent placenta dispositioned for a scheduled delivery. The primary outcome will be assessed by comparing the composite neonatal morbidity and composite maternal morbidity between the two groups (delivery at 34 versus 36 weeks gestational age). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02635412
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact
Status Withdrawn
Phase N/A
Start date March 2016
Completion date March 2018
View Details
See also
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