Chronic Indwelling Foley and Catheter Associated Trauma (CIF-CAT) Study

Bladder Infections and Inflammations Clinical Trial

Official title:

Chronic Indwelling Foley and Catheter Associated Trauma (CIF-CAT) Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03790826
• Other study ID #: CIFCAT-001
• Status: Not yet recruiting
• Phase: N/A
• Start date: April 2019
• Est. completion date: March 2021

Study information

• Verified date: March 2019
• Source: Nellie Medical, LLC
• Contact: James A Greenberg, MD
• Phone: 781-910-1968
• Email: JAGREENBERG[@]partners.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To determine whether an indwelling low profile Kohli Atraumatic Catheter causes less macro-morphologic inflammation and edema to the bladder mucosa than a traditional indwelling Foley catheter as assess by computerized image analysis.

Description:

The Kohli Atraumatic Catheter similarly aims to reduce bladder mucosal trauma with its low profile pancake shaped balloon versus the ovoid balloon of a traditional Foley catheter. The Kohli Atraumatic Catheter has a short, opened-ended tip that minimally protrudes through a patented low-profile donut-shaped balloon. The combination of the low profile and reduced tip length prevents the catheter from contacting the bladder walls and thereby minimize disruption of the bladder surface mucus layer and trauma to the urothelium - theoretically reducing the chance of bacterial invasion. A trial in which sheep were randomized to a traditional indwelling Foley catheter or a prototype Kohli Atraumatic Catheter demonstrated a dramatic reduction in both bladder wall trauma and edema. The ulcerated area dropped from 7.2% to 1.8% (75%) and the edema from 26.9% to 13.0% (52%).

Statistical Analysis To compare the effects of 2 catheter types, data will be analyzed using the general linear models tools from SAS/STAT software and presented as means ± standard error of the mean. The model will include 2 catheter types, inflamed vs non-inflamed areas, and their interactions.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 25
• Est. completion date: March 2021
• Est. primary completion date: December 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Men or Women older than age 18

• Indwelling Foley urinary catheter for at least 30 days prior to entry with anticipation for continued indwelling urinary catheterization for at least 30 days after entry into the study.

Exclusion Criteria:

• Inability to provide informed consent

• Unwilling or medically inappropriate for cystoscopy

Related Conditions & MeSH terms

• Bladder Infections and Inflammations
• Cystitis
• Inflammation

Intervention

Device:
• cystoscopy
Comparison of bladder mucosa via cystoscopy.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Nellie Medical, LLC

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Bladder mucosa damage assessment via computerized image analysis	Macro-morphologic inflammation and edema assessment of bladder mucosa using computerized image analysis.; Image Analysis Technique Image of each bladder will be analyzed using FLIR Research IR Software (FLIR Systems Inc., Wilsonville, OR) to determine the proportion of inflamed areas characterized by red surface including hemorrhage and ulceration, and edema (eg, swollen smooth surface) out of total bladder area.	30 days
Secondary	Bladder mucosa damage urologist visual assessment	Visual macro-morphologic inflammation and edema assessment of bladder mucosa by experienced urologists familiar with the assessment of bladder diseases. Images and videos from a first visit where the traditional Foley catheter has been in place will be compared to those from a subsequent cystoscopy. Urologists will be blinded as to the catheter associated with each block of images captured during the cystoscopy.	30 days
Secondary	Patient discomfort via Numeric Pain Rating Scale	A numeric pain rating scale chart will be completed by each patient for comparison of patient discomfort with a traditional indwelling Foley catheter in patients with chronic indwelling Foley catheters. The scale runs from 0 "No Pain" to 5 "Moderate Pain" and 10 "Worst Possible Pain." More information on the scale can be seen here "https://www.physio-pedia.com/Numeric_Pain_Rating_Scale" There are no Subscales and the marked score for first assessment will be compared to 2nd assessment to assess any changes in patient comfort with the two different catheters.	30 days