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Detecting Urinary Retention After Child Birth With a Ultrasound Scanner
This study has been completed.
Sponsored by: Rikshospitalet HF
Information provided by: Rikshospitalet HF
ClinicalTrials.gov Identifier: NCT00418223
  Purpose

The purpose of this study is a systematical registration of ultrasound measurements and urinary volume after catheterization. Based on these pairs of measurements we will calculate the reliability of ultrasound compared with catheter volume.


Condition Phase
Urinary Retention
Phase IV

MedlinePlus related topics: Ultrasound
U.S. FDA Resources
Study Type: Observational
Study Design: Prospective
Official Title: Detecting Urinary Retention After Child Birth With a Ultrasound Scanner

Further study details as provided by Rikshospitalet HF:

Estimated Enrollment: 100
Study Start Date: November 2005
Estimated Study Completion Date: February 2007
  Eligibility

Ages Eligible for Study:   18 Years to 50 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Women with suspected urinary retention
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00418223

Locations
Norway
Rikshospitalet-Radiumhospitalet HF
Oslo, Norway, 0027
Sponsors and Collaborators
Rikshospitalet HF
Investigators
Study Director: Leiv A Rosseland, MD Rikshospitalet HF
  More Information

Publications:
Study ID Numbers: Lukasse-2006, S-06412a
Study First Received: January 2, 2007
Last Updated: May 20, 2008
ClinicalTrials.gov Identifier: NCT00418223  
Health Authority: Norway: Directorate for Health and Social Affairs;   Norway: Norwegian Social Science Data Services;   Norway: The National Committees for Research Ethics in Norway

Keywords provided by Rikshospitalet HF:
Urinary retention
Child birth
Catheterization
Ultrasound

Study placed in the following topic categories:
Urologic Diseases
Urination Disorders
Urinary Retention

ClinicalTrials.gov processed this record on January 14, 2009