Uroflow Measurements in Healthy Volunteers

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

Completed

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Key information

Conditions

Healthy

Age range

18 year–65 year

Sex eligibility

Female

Study type

Observational

Primary location

Urogynecology and Reconstructive Pelvic Surgery Center

Rochester, New York, 14623, United States

About this study

see above

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

Voided Volume

Time frame: March 2008

Volume of spontaneous void
Maximal Flow Rate

Time frame: March 2008

Maximal uroflow of spontaneous subject voids

Sponsors and collaborators

Lead sponsor

University of Rochester

Other

Registry information

Important dates

Study start: 2008
Primary completion: 2008
Study completion: 2008
First posted: Jul 14, 2008
Registry last updated: Feb 6, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed