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Evaluation of Post-voiding Residual Urine: a Before-after, Post-partum Study — RPM-Eval  

Postpartum Women Clinical Trial

Official title:
Evaluation of Post-voiding Residual Urine: a Before-after, Post-partum Study

Clinical Trial Summary

The primary objective of this study is to evaluate the impact of systematic catheter-drainage of urine for parturient women immediately in the delivery room on the occurrence of post-voiding urine residue.

Clinical Trial Description

Secondarily, we will evaluate the impact of systematic catheter-drainage of urine for parturient women immediately in the delivery room on the occurrence of acute urine retention (first voiding volume > 500cc) and on post-partum bacteriuria rates. ;

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02597413
Study type Observational
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Completed
Phase N/A
Start date September 2015
Completion date September 2015
View Details
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