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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 weeks
Treatment ~ Varies
Follow Up ~up to 24 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 24 months for reporting.

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 more

Trial 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.

Find a Location

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

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~14 spots leftby Apr 2025