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NCT04030377 Clinical Trial

Postop Catheterization for Urinary Retention

Urinary Retention Clinical Trial

Official title:
Treatment of Postoperative Urinary Retention - WHAT DO WOMEN WANT?

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT04030377
Other study ID # EH11-096
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date April 2010
Est. completion date February 20, 2015

Study information
Verified date July 2019
Source NorthShore University HealthSystem
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

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.

Recruitment information / eligibility
Status Terminated
Enrollment 47
Est. completion date February 20, 2015
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States NorthShore University HealthSystem Skokie Illinois

Sponsors (1)
Lead Sponsor Collaborator
NorthShore University HealthSystem

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Patient satisfaction with choice of catheterization method Assessed through post-operative questionnaire completion 2 weeks after index procedure
Secondary Assessment of complication rates Comparison of complication rates between intermittent vs. indwelling catheterization: data derived from review of participant medical record 2 weeks after index procedure
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Terminated NCT00563654 - Randomized Trial Comparing Alfuzosin GITS 10 mg Daily With Placebo for Trial Without Catheter in Acute Urinary Retention With Long Term Follow up N/A
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Terminated NCT04682366 - The Effect of Tamsulosin on Postoperative Urinary Retention Phase 4