Uroflow Measurements in Urogynecology Patients Compared to Healthy Female Volunteers

To compare uroflowmetry measurements of patients undergoing urodynamic testing as part of an incontinence work-up in an urogynecology practice to healthy female volunteers.

Completed

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Key information

Conditions

Urogynecology

Age range

25 year–60 year

Sex eligibility

Female

Study type

Observational

Primary location

University of Rochester

Rochester, New York, 14642, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

All patients who underwent urodynamics at the urogynecology clinic during the past 12 months
Voids larger than 50 mls.

Exclusion criteria

History of pelvic organ prolapse, incomplete bladder emptying, and voids less than 50cc.

Treatment and study plan

Primary outcomes

Voiding variables of patients will be compared to those of healthy female volunteers collected from another study.

Sponsors and collaborators

Lead sponsor

University of Rochester

Other

Registry information

Important dates

Study start: 2008
Primary completion: 2008
Study completion: 2008
First posted: Jun 12, 2009
Registry last updated: Dec 16, 2009

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.

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Completed