Uroflow Measurements in Healthy Volunteers

NCT ID: NCT00714389

Last Updated: 2013-02-06

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

12 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-02-29

Study Completion Date

2008-03-31

Brief Summary

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The goal of this study to determine normal values for certain urinary measurements in order to better understand voiding dysfunction in women.

Detailed Description

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see above

Conditions

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Healthy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Healthy volunteers/employees
* Normal voiding function.
* Willing to participate.

Exclusion Criteria

* Subjects currently receiving treatment for any lower urinary tract condition or having any voiding difficulty.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Rochester

OTHER

Sponsor Role lead

Responsible Party

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Gunhilde Buchsbaum

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Gunhilde Buchsbaum, MD

Role: PRINCIPAL_INVESTIGATOR

University of Rochester

Locations

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Urogynecology and Reconstructive Pelvic Surgery Center

Rochester, New York, United States

Site Status

Countries

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United States

Other Identifiers

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22847

Identifier Type: -

Identifier Source: org_study_id

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