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Clinical Trial Summary

A study to compare maternal and perinatal outcome between 4 and 6 cm cervical dilatation at amniotomy.


Clinical Trial Description

Low risk women with singleton pregnancy are recruited. There are two groups which are 4 and 6 cm cervical os dilatation. The intrapartum management and labour outcomes are documented. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05339399
Study type Observational
Source National University of Malaysia
Contact
Status Completed
Phase
Start date May 1, 2021
Completion date February 10, 2022

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