Indwelling Urinary Catheterization Versus Clean Intermittent Catheterization for the Short-term Management of Hospitalized Patients With Transient Acute Urinary Retention

NCT ID: NCT02942641

Last Updated: 2016-10-24

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

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-06-30

Study Completion Date

2015-05-31

Brief Summary

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Objective: Acute urinary retention (AUR) is a common problem in hospitalized patients. Either indwelling urethral catheterization or clean intermittent catheterization (CIC) can be the choice of treatment. In chronic urinary retention, most physicians prefer CIC to chronic indwelling urethral catheter on the basis of the claim that the rate of catheter-associated urinary tract infection (CAUTI) is lower.

Method: The patients were randomized into indwelling urethral catheter and CIC groups. The primary outcomes of the study were catheter-associated asymptomatic bacteriuria and CAUTI. The secondary outcomes were pain, hematuria, cloudy urine, and quality of life.

Detailed Description

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We queried the hospitalized patients in Ramathibodi Hospital who developed first-time AUR from June 2014 to May 2015. Patients under 18 years of age with a history of urinary retention, urinary tract infection, and poor compliance were excluded from this study. All the patients gave their written informed consents. The patients were randomly divided into two groups depending on the type of assigned intervention: CIC and indwelling urethral catheter groups.

All the patients were followed up after 2 weeks; urinalysis and urine culture were obtained at the time of AUR and whenever the patients developed UTI-associated symptoms. The patients with positive urine culture at the time of AUR were excluded from the study.

Conditions

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Urinary Retention

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Indwelling urethral catheterization (Foley)

Foley catheter as the intervention.

Group Type EXPERIMENTAL

Indwelling urethral catheterization (Foley)

Intervention Type PROCEDURE

Hospitalized patients who developed first-time AUR were randomly divided into two groups depending on the type of assigned intervention: CIC and indwelling urethral catheter groups.

Patients in this group received indwelling urethral catheter as the intervention.

Foley

Intervention Type DEVICE

Clean intermittent catheterization (CIC)

CIC as the intervention .

Group Type EXPERIMENTAL

Clean intermittent catheterization (CIC)

Intervention Type PROCEDURE

Hospitalized patients who developed first-time AUR were randomly divided into two groups depending on the type of assigned intervention: CIC and indwelling urethral catheter groups.

Patients in this group received CIC as the intervention.

Interventions

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Indwelling urethral catheterization (Foley)

Hospitalized patients who developed first-time AUR were randomly divided into two groups depending on the type of assigned intervention: CIC and indwelling urethral catheter groups.

Patients in this group received indwelling urethral catheter as the intervention.

Intervention Type PROCEDURE

Clean intermittent catheterization (CIC)

Hospitalized patients who developed first-time AUR were randomly divided into two groups depending on the type of assigned intervention: CIC and indwelling urethral catheter groups.

Patients in this group received CIC as the intervention.

Intervention Type PROCEDURE

Foley

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Hospitalized patients in Ramathibodi Hospital who developed first-time AUR from June 2014 to May 2015.

Exclusion Criteria

* Patients under 18 years of age
* History of urinary retention
* Urinary tract infection
* Poor compliance
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ramathibodi Hospital

OTHER

Sponsor Role lead

Responsible Party

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Dr. Pocharapong Jenjitranant

Dr. Pocharapong Jenjitranant

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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095920

Identifier Type: -

Identifier Source: org_study_id

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