Disposable Stress Urinary Incontinence Pessary Device Study
Completed · Not applicable
Conditions studied: Stress Urinary Incontinence
In brief
This study is an interventional, single arm, multi-center study. It will be conducted at sites in the northeastern United States. The protocol will be approved by Chesapeake IRB or applicable local IRBs. The sample size will consist of approximately 50 participants. Participants will undergo an initial control period in which preweighed pads will be worn for 7 consecutive days for 12 hours. This will be followed by device usage for 14 consecutive days where participants will wear both device and preweighed pads simultaneously. for 12 hours.
Key facts
- Study ID
- NCT03323723
- Run by
- Rinovum Women's Health, Inc.
- People needed
- 73
- Starts
- 2017-10-16
- Expected to finish
- 2018-05-01
- Last updated by the study team
- 2019-05-16
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- • Provision of signed and dated informed consent form
- Literacy must be in English (able to read and understand Informed Consent)
- Stated willingness to comply with all study procedures and availability for the duration of the study
- Female, aged >18
- Be in generally good heath as determined by the Investigator
- Have a physician diagnosis of SUI that occurred prior to or during the screening visit of this study
- Have a > 3-month history of experiencing > 3 episodes of SUI per week
- Be willing to use the investigational pessary device for the control of urinary incontinence
- Have experience with wearing a tampon
- The most recent Pap smear is normal within 36 months.
You may not qualify if…
- • Is pregnant, or planning to become pregnant during the study
- Has been physician diagnosed with urge urinary incontinence or mixed urinary incontinence prior to or during the screening visit for this study
- Is post-partum within 3 months
- Has had an intrauterine device (IUD) placement of less than 6 months
- Has self-reported difficulty emptying her bladder;
- Has a history of Toxic Shock Syndrome (TSS) or symptoms consistent with TSS;
- Has experienced difficulty inserting or wearing an intra-vaginal device, including a tampon;
- Has had vaginal surgery, perineal surgery, uterine surgery, or abortion (spontaneous or induced) within the past 3 months;
- Has any Screening laboratory value outside the laboratory reference range considered clinically significant by the Investigator which could impact the safety of the participant or the outcome of the study
- Has an active urinary tract infection or vaginal infection requiring treatment
- If for any reason, the Investigator decides that the participant should not participate in the study.
- Class III Obesity (BMI> 40.0 kg/m2)
- Advanced prolapse
- Fit assessment is not successful during screening visit
Where it is running
- Cleveland Clinic — Cleveland, Ohio, United States
- Allegheny Health Network/East Suburban OB/GYN — Monroeville, Pennsylvania, United States
- West Virginia University Medicine — Morgantown, West Virginia, United States
Full record on ClinicalTrials.gov
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