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Postop Catheterization for Urinary Retention

NCT ID: NCT04030377

Last Updated: 2019-07-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Total Enrollment

47 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-04-30

Study Completion Date

2015-02-20

Brief Summary

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

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Detailed Description

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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.

Conditions

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Urinary Retention

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* Patients who cannot read, comprehend, and write in English
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Endeavor Health

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sylvia M Botros, MD

Role: STUDY_DIRECTOR

Endeavor Health

Locations

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NorthShore University HealthSystem

Skokie, Illinois, United States

Site Status

Countries

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United States

Other Identifiers

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EH11-096

Identifier Type: -

Identifier Source: org_study_id

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