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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
Nellie Medical, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Bladder Infections and Inflammations focused on measuring bladder mucosal trauma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

    First Posted
    December 27, 2018
    Last Updated
    March 25, 2019
    Sponsor
    Nellie Medical, LLC
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    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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