Detecting Urinary Retention After Child Birth With a Ultrasound Scanner

NCT ID: NCT00418223

Last Updated: 2011-04-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-11-30

Study Completion Date

2007-02-28

Brief Summary

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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.

Detailed Description

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Conditions

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Urinary Retention

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Women with suspected urinary retention
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Oslo University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Oslo University Hospital

Principal Investigators

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Leiv A Rosseland, MD

Role: STUDY_DIRECTOR

Oslo University Hospital

Locations

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Rikshospitalet-Radiumhospitalet HF

Oslo, , Norway

Site Status

Countries

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Norway

References

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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. doi: 10.1080/00016340701621478.

Reference Type BACKGROUND
PMID: 17851812 (View on PubMed)

Other Identifiers

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S-06412a

Identifier Type: -

Identifier Source: secondary_id

Lukasse-2006

Identifier Type: -

Identifier Source: org_study_id

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