Assessment of Third Trimester Post-void Residual and Validation of Bladder Scanner in Pregnancy and Post-partum
NCT ID: NCT00782730
Last Updated: 2013-06-13
Study Results
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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COMPLETED
35 participants
OBSERVATIONAL
2008-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Bladder Scan Group
Patients who agree to enroll in the trial and allow their known bladder volumes and residual bladder volumes to be measured by actual volumes retrograde instilled, and also by bladder scanner ultrasound.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Having a non-emergent Cesarean Delivery or labor epidural placed.
Exclusion Criteria
* Emergent Cesarean delivery.
* No epidural labor analgesia.
18 Years
FEMALE
No
Sponsors
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West Virginia University
OTHER
Responsible Party
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Michael Stitely
Adjunct Associate Professor
Principal Investigators
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Michael L Stitely, MD
Role: PRINCIPAL_INVESTIGATOR
West Virginia University
Locations
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West Virginia University
Morgantown, West Virginia, United States
Countries
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Other Identifiers
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H-20862
Identifier Type: -
Identifier Source: org_study_id
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