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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02597413

Acronym

RPM-Eval

Enrollment

Registered

2015-11-05

Start date

2015-09-30

Completion date

2015-09-30

Last updated

2016-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Women

Brief 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.

Detailed 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.

Interventions

PROCEDURECatheterization

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

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
Presence/absence of a post-voiding residue	Day 0 to Day 2 (just after first voiding)	Assessed just after the first post-partum voiding.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026