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Clinical Trial Summary

To compare the efficacy of the route and timing of oxytocin administration for Active management of third stage of labour (AMTSL).


Clinical Trial Description

Our objective is to determine the most efficient route and timing of oxytocin administration by measuring the duration of third stage of labour, quantitative blood during the first hour after delivery and comparing haemoglobin and haematocrit changes and the need for additional interventions in patients who had either a spontaneous labour or received labour augmentation with oxytocin. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject)


Related Conditions & MeSH terms


NCT number NCT01954186
Study type Interventional
Source Etlik Zubeyde Hanim Womens' Health and Teaching Hospital
Contact
Status Completed
Phase N/A
Start date January 2010
Completion date December 2010

See also
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