Viewing Study NCT02942641



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Last Modification Date: 2024-10-26 @ 12:12 PM
Study NCT ID: NCT02942641
Status: COMPLETED
Last Update Posted: 2016-10-24
First Post: 2016-10-19

Brief Title: Indwelling Urinary Catheterization Versus Clean Intermittent Catheterization for the Short-term Management of Hospitalized Patients With Transient Acute Urinary Retention
Sponsor: Ramathibodi Hospital
Organization: Ramathibodi Hospital

Study Overview

Official Title: Indwelling Urinary Catheterization Versus Clean Intermittent Catheterization for the Short-term Management of Hospitalized Patients With Transient Acute Urinary Retention A Prospective Randomized Trial
Status: COMPLETED
Status Verified Date: 2016-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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: 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None