Chronic Indwelling Foley and Catheter Associated Trauma (CIF-CAT) Study
Primary Purpose
Bladder Infections and Inflammations
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
cystoscopy
Sponsored by
About this trial
This is an interventional basic science trial for Bladder Infections and Inflammations focused on measuring bladder mucosal trauma
Eligibility Criteria
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
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Cystoscopic Inspection
Arm Description
Comparison of bladder damage with traditional Foley catheter and the Kohli Atraumatic catheter. Interventions: cystoscopy
Outcomes
Primary Outcome Measures
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.
Secondary Outcome Measures
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.
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.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03790826
Brief Title
Chronic Indwelling Foley and Catheter Associated Trauma (CIF-CAT) Study
Official Title
Chronic Indwelling Foley and Catheter Associated Trauma (CIF-CAT) Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Unknown status
Study Start Date
April 2019 (Anticipated)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
March 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nellie Medical, LLC
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief 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.
Detailed 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Infections and Inflammations
Keywords
bladder mucosal trauma
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
25 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Cystoscopic Inspection
Arm Type
Experimental
Arm Description
Comparison of bladder damage with traditional Foley catheter and the Kohli Atraumatic catheter.
Interventions: cystoscopy
Intervention Type
Device
Intervention Name(s)
cystoscopy
Intervention Description
Comparison of bladder mucosa via cystoscopy.
Primary Outcome Measure Information:
Title
Bladder mucosa damage assessment via computerized image analysis
Description
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.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Bladder mucosa damage urologist visual assessment
Description
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.
Time Frame
30 days
Title
Patient discomfort via Numeric Pain Rating Scale
Description
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.
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
James A Greenberg, MD
Phone
781-910-1968
Email
JAGREENBERG@partners.org
First Name & Middle Initial & Last Name or Official Title & Degree
Ronald Adams, MSME
Phone
5089445166
Email
ron@cystosure.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Chronic Indwelling Foley and Catheter Associated Trauma (CIF-CAT) Study
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