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Solid State vs. Balloon Esophageal Catheter for Estimation of Pleural Pressure

Primary Purpose

Respiratory Failure, Mechanical Ventilation

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
intelligent Esophageal Pressure Catheter (iEPC)
Sponsored by
Erasmus Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Respiratory Failure focused on measuring Esophageal manometry, Respiratory monitoring, Mechanical ventilation, Pleural pressure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Signed informed consent Patient requiring mechanical ventilation at the ICU following cardiothoracic or abdominal surgery Age ≥ 18 year Exclusion Criteria: Pregnancy Upper airway/esophageal/mouth or face pathology (i.e. recent surgery, esophageal varices, diaphragmatic hernia) Nasal bleeding within the last <2 weeks Presence of pneumothorax Use of anticoagulants that increase the risk of catheter insertion

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Esophageal manometry using a solid state sensor vs. balloon catheter

    Arm Description

    Placement of both a solid state and balloon esophageal pressure (Pes) catheter. Pes recordings of these catheters will be acquired simultaneously during both controlled mechanical ventilation and assisted mechanical ventilation, for 10-15 minutes per phase. Ventilator settings/protocol will be as per standard-of-care.

    Outcomes

    Primary Outcome Measures

    Difference in absolute Pes-derived parameters obtained by solid state catheter vs. balloon catheter.
    Absolute Pes value (in cmH2O) at end-expiration and at peak inspiration (based on flow recordings) will be recorded.
    Difference in relative Pes-derived parameters obtained by solid state catheter vs. balloon catheter.
    Relative Pes value (cmH2O) will be measured as the inspiratory amplitude in Pes.

    Secondary Outcome Measures

    Full Information

    First Posted
    April 3, 2023
    Last Updated
    September 6, 2023
    Sponsor
    Erasmus Medical Center
    Collaborators
    Pulmotech B.V.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05817968
    Brief Title
    Solid State vs. Balloon Esophageal Catheter for Estimation of Pleural Pressure
    Official Title
    Comparison of a Solid State Versus Balloon Esophageal Catheter for Estimation of Pleural Pressure in Surgical ICU Patients
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    October 2023 (Anticipated)
    Primary Completion Date
    January 2024 (Anticipated)
    Study Completion Date
    February 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Erasmus Medical Center
    Collaborators
    Pulmotech B.V.

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Measurements of esophageal pressure (Pes) as surrogate for pleural pressure are routinely performed in selected ICU patients to facilitate lung-protective ventilation and assess breathing effort. Pes is clinically measured via a nasogastric esophageal catheter. Current techniques involve balloon catheters but have some important disadvantages as they could deflate over time and require a very precise positioning and filling volume. A solid-state sensor does not have disadvantages associated with balloon catheters and may therefore be a useful alternative in clinical practice. This method-comparison study in adult mechanically ventilated ICU patients evaluates the accuracy of Pes measured using an esophageal catheter with a solid-state sensor as compared to a balloon catheter as reference standard.
    Detailed Description
    Measurements of esophageal pressure (Pes) as surrogate for pleural pressure are routinely performed in selected ICU patients to facilitate lung-protective ventilation and assess breathing effort. Pes is clinically measured via a nasogastric esophageal catheter. Current techniques involve balloon catheters but have some important disadvantages as they could deflate over time and require a very precise positioning and filling volume. A solid state sensor does not have disadvantages associated with balloon catheters and may therefore be a useful alternative in clinical practice. This method-comparison study in adult mechanically ventilated ICU patients evaluates the accuracy of Pes measured using an esophageal catheter with a solid-state sensor as compared to a balloon catheter as reference standard. Subjects will receive a standard balloon esophageal catheter and a solid-state pressure catheter for simultaneous measurements of Pes. Study population will be post-surgical ICU patients. Measurements will be performed during clinical mechanical ventilation settings which include a first phase of passive controlled ventilation (patient is still sedated after surgery) as well a phase of partially-assisted ventilation where the patient's breathing effort has resumed and is assisted by the ventilator. During both phases, 10-15 minutes of tidal breathing will be recorded.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Respiratory Failure, Mechanical Ventilation
    Keywords
    Esophageal manometry, Respiratory monitoring, Mechanical ventilation, Pleural pressure

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    Method comparison study; participants serve as their own control
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    16 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Esophageal manometry using a solid state sensor vs. balloon catheter
    Arm Type
    Experimental
    Arm Description
    Placement of both a solid state and balloon esophageal pressure (Pes) catheter. Pes recordings of these catheters will be acquired simultaneously during both controlled mechanical ventilation and assisted mechanical ventilation, for 10-15 minutes per phase. Ventilator settings/protocol will be as per standard-of-care.
    Intervention Type
    Device
    Intervention Name(s)
    intelligent Esophageal Pressure Catheter (iEPC)
    Other Intervention Name(s)
    Solid state esophageal pressure catheter, PulmoTech B.V.
    Intervention Description
    Placement of the iEPC nasogastric catheter with solid state sensor for esophageal manometry. Comparator: Esophageal balloon catheter (NutriVent).
    Primary Outcome Measure Information:
    Title
    Difference in absolute Pes-derived parameters obtained by solid state catheter vs. balloon catheter.
    Description
    Absolute Pes value (in cmH2O) at end-expiration and at peak inspiration (based on flow recordings) will be recorded.
    Time Frame
    30 minutes
    Title
    Difference in relative Pes-derived parameters obtained by solid state catheter vs. balloon catheter.
    Description
    Relative Pes value (cmH2O) will be measured as the inspiratory amplitude in Pes.
    Time Frame
    30 minutes

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Signed informed consent Patient requiring mechanical ventilation at the ICU following cardiothoracic or abdominal surgery Age ≥ 18 year Exclusion Criteria: Pregnancy Upper airway/esophageal/mouth or face pathology (i.e. recent surgery, esophageal varices, diaphragmatic hernia) Nasal bleeding within the last <2 weeks Presence of pneumothorax Use of anticoagulants that increase the risk of catheter insertion
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Annemijn Jonkman, PhD
    Phone
    010-7035142
    Email
    a.jonkman@erasmusmc.nl
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Annemijn Jonkman, PhD
    Organizational Affiliation
    Erasmus Medical Center
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Leo Heunks, PhD
    Organizational Affiliation
    Erasmus Medical Center
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Solid State vs. Balloon Esophageal Catheter for Estimation of Pleural Pressure

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