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

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.

Completed

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Key information

Conditions

Postpartum Women

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

CHRU de Nîmes - Hôpital Universitaire Carémeau

Nîmes, 30029, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Paturient women admitted to the delivery room

Exclusion criteria

Patients who have been catheterized during the third trimester of the current pregnancy
History of surgery on the urinary tract

Treatment and study plan

Catheterization

Procedure

Women in this group will be systematically catheterized before leaving the delivery room.

Primary outcomes

Presence/absence of a post-voiding residue

Time frame: Day 0 to Day 2 (just after first voiding)

Assessed just after the first post-partum voiding.

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nīmes

Other

Registry information

Acronym: RPM-Eval

Important dates

Study start: 2015
Primary completion: 2015
Study completion: 2015
First posted: Nov 5, 2015
Registry last updated: May 24, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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Completed