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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03785262
Other study ID # 113221
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date January 30, 2019
Est. completion date December 30, 2023

Study information

Verified date January 2024
Source Lawson Health Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Uroshield device is a commercially available device with two parts: a disposable actuator which attaches to the external portion of the catheter and a portable battery. The device sends out low-frequency ultrasound waves which run along the surfaces of the catheter. These acoustic waves prevent bacteria from adhering to the catheter and prevent the formation of biofilm. Our objective is to conduct a pilot study to determine if the UroShield device can reduce bacteriuria and catheter biofilm formation among neurogenic bladder patients with an indwelling catheter, as well as improve urinary quality of life and symptoms.


Recruitment information / eligibility

Status Terminated
Enrollment 6
Est. completion date December 30, 2023
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. >18 years of age 2. Spinal cord injury (>1 year), multiple sclerosis (>1 year), spina bifida, parkinsons (>1 year) 3. Indwelling catheter (urethral or suprapubic) for >3 months, and used as primary bladder management mechanism 4. >1 urinary tract infection in the last 12 months Exclusion Criteria: 1. Intravesical botox in the last 6 months 2. Chronic antibiotic suppressive therapy 3. Active symptomatic UTI on day of randomization 4. Unable to understand written and spoken English 5. Prior/current utilization of the Uroshield device

Study Design


Intervention

Device:
Uroshield
The Uroshield device sends out low-frequency ultrasound waves which run along the surface of the catheter.
Sham Uroshield
The sham Uroshield device is identical to the active machine, but it does not send out low-frequency ultrasound waves along the surface of the catheter.

Locations

Country Name City State
Canada St Josephs Hospital London Ontario

Sponsors (1)

Lead Sponsor Collaborator
Lawson Health Research Institute

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bacteriuria Proportion with bacteriuria >10^5 cfu at day 30 30 days
Secondary Neurogenic bladder symptom score (NBSS) Validated symptom score that measures symptoms related to neurogenic bladder dysfunction and urinary quality of life. Total scale ranges from 0-74, and a lower number is considered a better outcome and represents lower symptom burden. 30 days
Secondary Patient subjective rating of amount of sediment/debris at the end of the 30 days 30 days
Secondary Total bacterial cell counts 30 days
Secondary Microbiome comparison of biofilms 30 days
Secondary Scanning electron microscopy of biofilms 30 days
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