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Clinical Trial Summary

To determine the effect in the post operative period of early feeding (4 hours after surgery) vs. traditional management (feeding 12 hours after surgery) in uncomplicated cesarean section.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT02332278
Study type Interventional
Source Saint Thomas Hospital, Panama
Contact
Status Completed
Phase N/A
Start date June 2014
Completion date December 2014

See also
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