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The Effect of Hyoscine-N-butylbromide (HBB, Buscopan) in Augmented Labour Among Primigravidae

Labor Long Clinical Trial

Official title:
A Randomised Control Study: The Effect of Hyoscine-N-butylbromide (HBB, Buscopan) in Augmented Labour Among Primigravidae

Clinical Trial Summary

This study compares the duration of active phase of labour in women who received buscopan and those who don't.

Clinical Trial Description

A randomised control study involving primigravida in labour who require pitocin augmentation. Once patient require augmentation, patient will be randomised into intervention group (receiving intravenous buscopan 1ml or 20mg) and control group (intravenous normal saline 1ml). Both fluids are colourless. The primary outcome is duration from augmentation to os fully. The secondary outcome are to look on mode of delivery particularly any caesarean section due to failure to poor progress, maternal side effect (dry mouth and tachycardia) and baby outcome (apgar score and neonatal intensive care unit admission) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04349722
Study type Interventional
Source National University of Malaysia
Contact
Status Completed
Phase Phase 4
Start date December 1, 2019
Completion date June 30, 2020
View Details
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