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Intravaginal Devices for Urinary Incontinence

N/A
Recruiting
Led By Linda McLean
Research Sponsored by University of Ottawa
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Regularly (≥ 1 per week) experience urine leakage while running and report ≤1 urine leakage episode per month not associated with exercise
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks; follow-up at 4, 12 and 24 weeks later.
Awards & highlights

Study Summary

This trial found that 1 in 5 women experience urine leakage while exercising. Exercise is important and it's recommended to look for alternatives to manage this condition to maintain physical and mental health.

Who is the study for?
This trial is for cis-female runners over 18 who can run 5 km in under 50 minutes at least twice a week and have experienced urine leakage while running regularly. They should not have urogenital surgery history, neurologic disorders, recent pregnancy, or conditions causing exercise-related risks.Check my eligibility
What is being tested?
The study tests if intravaginal devices like tampons or pessaries can help reduce urinary incontinence during running. It aims to find non-surgical ways to manage this condition that often leads women to limit their physical activities.See study design
What are the potential side effects?
Potential side effects of using intravaginal devices may include discomfort, increased risk of vaginal infections, and possible irritation. However, these will vary based on individual tolerance and proper use.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I often leak urine when running but rarely at other times.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks; follow-up at 4, 12 and 24 weeks later.
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 weeks; follow-up at 4, 12 and 24 weeks later. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Brisk walking and Running lower Urinary Tract Symptoms Questionnaire (BRUTS) score
International Consultation on Incontinence Questionnaire Female Lower Urinary Tract Symptoms Modules (ICIQ-FLUTS)
Intervention questionnaire
+3 more
Secondary outcome measures
Adherence to each intervention
Adverse events
Changes in bladder neck height
+5 more

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: Tampon InterventionExperimental Treatment1 Intervention
Participants randomized to this group will receive 60 regular Tampax tampons and will be instructed to use them each time they run over a 12-week period. The tampon should be used only while running and removed and discarded when the training is over.
Group II: Pessary InterventionExperimental Treatment1 Intervention
Participants randomized to this group will receive an Uresta Incontinence Pessary to use each time they run over a 12-week period. They will be instructed to use the pessary only while running and remove it and wash it with soap and water when the training is over. Uresta is a reusable and removable device made of hypoallergenic medical-grade resin that is inserted into the vagina to provide mechanical support. It comes with a starter kit with 3 different sizes which work for over 80% of women. Participants will be instructed on how to test the 3 sizes to find out which one is right for them.
Group III: Control GroupActive Control1 Intervention
Participants randomized to this group won't receive any intervention and will be asked to continue their running training as usual for 12-weeks. They will also be instructed to not begin any treatment for urinary incontinence until their reassessment. After 12-weeks, they will be reassessed and will be offered the opportunity to receive a pessary if they desire so.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Pelvic Floor Muscle Training (PFMT) is a common treatment for Urinary Incontinence (UI) that works by strengthening the pelvic floor muscles, which support the bladder and urethra. Enhanced muscle strength and endurance improve bladder control, reducing incontinence episodes. This matters for UI patients as it offers a non-invasive, low-risk method to manage symptoms, improve quality of life, and encourage continued physical activity, which is often limited by incontinence.

Find a Location

Who is running the clinical trial?

University of OttawaLead Sponsor
210 Previous Clinical Trials
268,102 Total Patients Enrolled
Linda McLeanPrincipal InvestigatorUniversity of Ottawa
2 Previous Clinical Trials
113 Total Patients Enrolled

Media Library

Pessary Intervention Clinical Trial Eligibility Overview. Trial Name: NCT05773378 — N/A
Urinary Incontinence Research Study Groups: Pessary Intervention, Tampon Intervention, Control Group
Urinary Incontinence Clinical Trial 2023: Pessary Intervention Highlights & Side Effects. Trial Name: NCT05773378 — N/A
Pessary Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT05773378 — N/A
~30 spots leftby Feb 2025