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Pessary
Cooper Surgical Ring Pessary with Incontinence Knob for Stress Incontinence
N/A
Recruiting
Led By Catherine Smith, MD
Research Sponsored by University of British Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 24 months
Awards & highlights
Study Summary
This study is evaluating whether a pessary can improve urinary leakage in pregnant women.
Eligible Conditions
- Stress Incontinence
- Pregnancy
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 24 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
PFDI-20 score difference and variance
Secondary outcome measures
Abdominal Pain
Bladder Diary
Delivery
+17 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: PessaryExperimental Treatment1 Intervention
Study Participants who are fitted with a pessary for urinary incontinence. This group will be given an information pamphlet on pelvic floor (Kegel) exercises in pregnancy and pessary use in pregnancy. They will continue to have standard antenatal care with their maternity provider.
Group II: ControlActive Control1 Intervention
Study Participants who do not receive a pessary. This group will be given an information pamphlet on pelvic floor (Kegel) exercises in pregnancy and will continue to have standard antenatal care with their maternity provider.
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Who is running the clinical trial?
University of British ColumbiaLead Sponsor
1,413 Previous Clinical Trials
2,466,901 Total Patients Enrolled
Catherine Smith, MDPrincipal InvestigatorUniversity of British Columbia
1 Previous Clinical Trials
90 Total Patients Enrolled
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