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TerminatedNCT04030377Updated Jul 24, 2019

Postop Catheterization for Urinary Retention

An observational study in Urinary Retention, sponsored by Endeavor Health. Terminated at 1 site in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-07-24.

Sponsored by Endeavor Health · Observational

Why this study was terminated
Insufficient enrollment, question addressed by other researchers
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
47
Ages
18 Years and older
Sex
Female
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Study summary

This study investigates patient's preference and satisfaction with choice of catheterization after surgical urogynecological procedures.

Read the detailed description

Preoperatively, the enrolled patient receives information about risks and benefits of three ways of bladder catheterization as means of management of postoperative urinary retention. Based on this information, the patient chooses her preferred way of postoperative catheterization in case she experiences acute urinary retention after surgery. After the surgery, those patients requiring catheterization postoperatively evaluate their experience in a postoperative questionnaire.

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Conditions studied

  • Urinary Retention

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03

In context

Urinary Retention

240 studies on the registry are indexed under Urinary Retention; 39 are open to participants now.

This study's enrollment of 47 is below the median of 100 across 44 observational studies indexed under Urinary Retention.

Browse Urinary Retention studies →

Lead sponsor

Endeavor Health is the lead sponsor of 111 studies on the registry; 34 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 9 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult women presenting to the urogynecology offices at NorthShore University HealthSystem with a urogynecologic diagnosis desiring surgical management.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All female patients who undergo urogynecological surgery procedures at NorthShore University HealthSystem and consent to participate

Exclusion criteria

Exclusion Criteria:

  • Patients who cannot read, comprehend, and write in English
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
47 participants (actual)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Patient satisfaction with choice of catheterization method

    Assessed through post-operative questionnaire completion

    Time frame: 2 weeks after index procedure

Secondary outcomes

  1. Assessment of complication rates

    Comparison of complication rates between intermittent vs. indwelling catheterization: data derived from review of participant medical record

    Time frame: 2 weeks after index procedure

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Study locations

1 site
  • NorthShore University HealthSystem
    Skokie, Illinois 60076, United States
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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Apr 2010 to primary completion in Dec 2014, 56 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 19, 2019
First posted
Jul 24, 2019
StartActual
Apr 2010
Primary completionActual
Dec 2014
CompletionActual
Feb 20, 2015
Last update
Jul 24, 2019
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 24, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04030377
Lead sponsor
Endeavor Health
Responsible party
Sponsor
First posted
Jul 24, 2019
Start date
Apr 2010
Primary completion
Dec 2014
Completion
Feb 20, 2015
Last update
Jul 24, 2019

Study contacts

Sylvia M Botros, MD
study director · Endeavor Health

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jul 2019. You cannot join it, but the record below documents what was studied.

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