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Clinical Trial Summary

Postpartum haemorrhage is a major contributor to maternal mortality in the developing world. The incidence is between 5 and 12% in Jamaica and varies depending on the route of delivery. Misoprostol is a uterotonic agent which has the potential to augment the effects of the standard parenteral oxytocic agents used as best practice in the active management of the third stage of labour, thereby reducing the risk of postpartum haemorrhage and its attendant complications.

The Aim of the study is twofold: to show that this additive effect translates to a reduced postpartum haemorrhage rate and secondly to demonstrate reduced side effects of misoprostol resulting from the lower dose and the powdered sublingual administration.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04044287
Study type Interventional
Source The University of The West Indies
Contact Carole Rattray, DM
Phone 876.927.1145
Email carole.rattray@uwimona.edu.jm
Status Recruiting
Phase Phase 3
Start date January 1, 2013
Completion date December 31, 2019

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