Extended Pessary Interval for Care (EPIC Study)

Sponsor
Unity Health Toronto (Other)
Overall Status
Unknown status
CT.gov ID
NCT01644214
Collaborator
Women's College Hospital (Other), Mount Sinai Hospital, Canada (Other)
13
1
2
40
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Study Details

Study Description

Brief Summary

Objectives: Pelvic organ prolapse (POP) is a common condition for which pessaries are commonly used in conservative treatment. Despite their prevalence, there is no literature to guide the management of pessaries. Our objective is to determine whether patients managed with a pessary for POP are more satisfied with follow-up at 3 or 6 month intervals and if there is any difference in complications rates between the two groups.

Hypothesis: The investigators hypothesize that there will be higher patient satisfaction in the group randomized to 6 month follow-up intervals and that there will be no difference in complication rates between the two follow-up groups.

Method: The investigators will conduct a prospective randomized control trial comparing patient satisfaction and complication rates between patients with pessaries randomized to either 3 or 6 month follow-up intervals over 1 year.

Condition or Disease Intervention/Treatment Phase
  • Other: 6 month follow up for pessary check in the clinic setting
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
13 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Extended Pessary Interval for Care (EPIC Study): Patient Preference for 3 Verus 6 Month Follow-up
Study Start Date :
Nov 1, 2016
Actual Primary Completion Date :
Nov 1, 2019
Anticipated Study Completion Date :
Mar 1, 2020

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Pessary Check at 3 months

Patients seen at 3 month intervals for pessary check-ups is the most common interval check in our clinic so this arm is considered the control group.

Experimental: 6 month Pessary Check

Those that will be seen at 6 month follow-up visits for pessary maintenance will be considered the experimental group of the study.

Other: 6 month follow up for pessary check in the clinic setting
The standard of care is considered to be pessary checks every 3 months, therefore those that are checked every 6 months will be considered to be in the intervention group.

Outcome Measures

Primary Outcome Measures

  1. Patient satisfaction [At 6 months from study enrollment]

    To determine if patients managed with a pessary for POP are more satisfied with follow-up at 6 or 12 weeks over a one year period.

  2. Patient satisfaction [At 12 months from study enrollment]

    To determine if patients managed with a pessary for POP are more satisfied with follow-up at 6 or 12 weeks over a one year period.

Secondary Outcome Measures

  1. Pessary associated complications [Checked at all follow-up visits (3 and 6 months, depending on study group)]

    To determine if there is a difference in complication rates associated with indwelling pessaries between those that are seen at 6 week intervals and those that are seen at 12 week intervals, over a one year time period.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Females with POP who have opted for conservative management with a pessary

  • Able to read and write English

  • First time pessary users

  • Successful fitting with a covered ring or Gellhorn pessary, as determined at the usual early follow-up visit 2-4 weeks after initial fitting (successful defined as: no expulsion on movement, squatting or valsalva, no urinary retention, no discomfort, and still retained pessary after 2 weeks)

  • Patients agree to use vaginal estrogen (either tablet or cream twice weekly) during the study period; patients may not use a vaginal estrogen ring since this requires changing every 3 months, and will interfere with the study follow-up schedule

Exclusion criteria:
  • Current presence of vaginal bleeding, vaginal abrasions or ulcers, or vaginal infection

  • Significant cognitive impairment

  • Pessary used for indication other than POP (ie. urinary incontinence)

  • Use of a pessary that is not a covered ring or Gellhorn (i.e exclude cube, donut, etc.)

  • Contraindications to vaginal estrogen

  • Unsuccessful pessary fitting (successful defined as: no expulsion on movement, squatting or valsalva, no urinary retention, no discomfort, and still retained pessary after 2 weeks)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Women's College Hospital/Mount Sinai Hospital Toronto Ontario Canada M5G 1Z5

Sponsors and Collaborators

  • Unity Health Toronto
  • Women's College Hospital
  • Mount Sinai Hospital, Canada

Investigators

  • Principal Investigator: Colleen D McDermott, MD, FRCSC, St. Michael's Hospital, Women's College Hospital, University of Toronto

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Unity Health Toronto
ClinicalTrials.gov Identifier:
NCT01644214
Other Study ID Numbers:
  • PessaryProtocol
First Posted:
Jul 19, 2012
Last Update Posted:
Dec 4, 2019
Last Verified:
Dec 1, 2019
Keywords provided by Unity Health Toronto
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 4, 2019