Bacteriuria and Indwelling Urinary Catheter.

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

196 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-05-24

Study Completion Date

2025-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Investigation of 1. The incidence of symptomatic bacteriuria during four weeks after removal of an IUC in inpatients at a rehabilitation clinic for patients ≥ 65 years compared with the incidence of symptomatic bacteriuria among inpatients not treated with an IUC and 2. For how long does ABU persist in inpatients at a rehabilitation clinic for patients

≥ 65 years during a follow-up time of four weeks after IUC-removal?

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Bacterial Interference for Prevention of Catheter-Associated UTI: Geriatric Pilot Study

NCT00554996

Urinary Tract Infection

COMPLETED PHASE1

REPLACE: The Impact of Catheter Replacement in Patients With Catheter-associated Urinary Tract Infection

NCT06936631

Catheter Associated Urinary Tract Infection

RECRUITING NA

Antibiotic Bladder Instillations vs. Oral Suppression for the Treatment of Recurrent Urinary Tract Infections

NCT04285320

Recurrent Urinary Tract Infection

UNKNOWN PHASE4

Open Prospective Study on Reduction of Bacteriuria Following Bladder Irrigation With Chlorhexidine

NCT01782404

Bacteriuria, Intermittent Catheterization

COMPLETED NA

Prevention of Catheter Associated Lower Urinary Infections Using the Oxys Indwelling Catheter

NCT02658903

Urinary Infections

UNKNOWN PHASE1

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Bacteriuria Asymptomatic Urinary Tract Infections

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Intervention group

Inpatients with an indwelling urinary catheter (IUC) at admission to a rehabilitation clinic for persons ≥65 years in Sweden. Intervention is removal of the IUC.

Indwelling urinary catheter

Intervention Type DEVICE

Removal of indwelling urinary catheter

Control group

Inpatients without an IUC at admission to a rehabilitation clinic for persons ≥65 years in Sweden

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Indwelling urinary catheter

Removal of indwelling urinary catheter

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Admission to a rehabilitation clinic for patients ≥ 65 years in Stockholm County, Sweden
* Ability to understand oral and written instructions in Swedish
* Ability to produce a voided urine-sample

Exclusion Criteria

* Severe cognitive failure and/or disability to understand oral and written instructions in Swedish according to the healthcare-personnel's judgment at the ward
* End-of-life care
* Physical disability to produce voided urine-samples
* Ongoing antimicrobial treatment for symptomatic bacteriuria

Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No