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NCT02597413 Clinical Trial

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

Postpartum Women Clinical Trial

— RPM-Eval  

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02597413
Other study ID # LOCAL/2015/MN-01
Secondary ID
Status Completed
Phase N/A
First received November 4, 2015
Last updated May 23, 2016
Start date September 2015
Est. completion date September 2015

Study information
Verified date May 2016
Source Centre Hospitalier Universitaire de Nimes
Contact n/a
Is FDA regulated No
Health authority France: Commission nationale de l'informatique et des libertés
Study type Observational

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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 88
Est. completion date September 2015
Est. primary completion date September 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Procedure:
• Catheterization
Women in this group will be systematically catheterized before leaving the delivery room.

Locations
Country Name City State
France CHRU de Nîmes - Hôpital Universitaire Carémeau Nîmes Cedex 09

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Presence/absence of a post-voiding residue Assessed just after the first post-partum voiding. Day 0 to Day 2 (just after first voiding) No
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