University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, 73104, United States
NCT Number: NCT03010800
This study will test the acute efficacy of an investigational device (Yoni.Fit) in a clinical trial of women with incontinence in a standardized set of challenges performed with and without the device in place.
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Notify Me25 year–65 year
Female
Interventional
Not applicable
Oklahoma City, Oklahoma, 73104, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Abbreviated Pad Test with Yoni.Fit first, then without Yoni.Fit.
Abbreviated Pad Test without Yoni.Fit, then with Yoni.Fit.
Time frame: An hour after finishing a liter of liquid
Comparison of urine weight of the pad without Yoni,Fit to the weight of the pad with Yoni.Fit controlling for the tare weight.
Watkins Conti Products. Inc.
Industry
Randomized, Crossover Feasibility Study of a Device to Prevent Female Urinary Stress Incontinence
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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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