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Clinical Trial Summary

Investigators will observe the incidence of post-cesarean nausea or vomiting and try to associate it with some risk factors.


Clinical Trial Description

A single prospective cohort of women submitted to cesarean section who received spinal anesthesia will be assessed for the proposed risk factors and the incidence of nausea or vomiting will be observed during the first 48 hours. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03171688
Study type Observational
Source Brasilia University Hospital
Contact
Status Completed
Phase
Start date May 1, 2016
Completion date November 1, 2018

See also
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