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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00418223
Other study ID # Lukasse-2006
Secondary ID S-06412a
Status Completed
Phase Phase 4
First received January 2, 2007
Last updated April 18, 2011
Start date November 2005
Est. completion date February 2007

Study information

Verified date April 2011
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway: Directorate of HealthNorway: Norwegian Social Science Data ServicesNorway:National Committee for Medical and Health Research Ethics
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date February 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Women with suspected urinary retention

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Norway Rikshospitalet-Radiumhospitalet HF Oslo

Sponsors (1)

Lead Sponsor Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Lukasse M, Cederkvist HR, Rosseland LA. Reliability of an automatic ultrasound system for detecting postpartum urinary retention after vaginal birth. Acta Obstet Gynecol Scand. 2007 Oct;86(10):1251-5. — View Citation

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