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Clinical Trial Summary

The aim of this study is to evaluate the effect of immediate oral hydration initiated within 2 hours after uncomplicated Caesarean section


Clinical Trial Description

The aim of this study is to evaluate the effect of immediate oral hydration initiated within 2 hours after uncomplicated Caesarean section on the following post-operative outcomes:

1. Post-operative nausea, vomiting, abdominal distention and abdominal cramps.

2. Return of intestinal movements.

3. Duration of intravenous fluid administration.

4. Duration of hospital stay.

5. Participant satisfaction ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03566498
Study type Interventional
Source Ain Shams University
Contact
Status Completed
Phase N/A
Start date August 1, 2016
Completion date April 2018

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