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Sugammadex Titration in Cardiac Surgery Patients

Primary Purpose

Coronary Artery Disease, Valvular Heart Disease, Aorta Disease

Status
Not yet recruiting
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Sugammadex administration
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Coronary Artery Disease focused on measuring neuromuscular blockade, sugammadex, monitoring, rocuronium, vecuronium

Eligibility Criteria

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

Inclusion Criteria

  • All cardiac surgery patients

Exclusion Criteria:

  • Allergic or other adverse response to sugammadex

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Cardiac surgery patients

    Arm Description

    Patients undergoing cardiac surgery

    Outcomes

    Primary Outcome Measures

    Total dose of sugammadex required to produce a train-of-four ratio of >0.9
    Sugammadex will be administered in 50 mg increments every 5 minutes until a train-of-four ratio is reached
    Twitch monitoring result prior to sugammadex administration
    The result of twitch monitoring prior to sugammadex administrative
    Duration of action of reversal
    The train-of-four ratio will be determined upon arrival to the ICU and every hour for 6 hours or until extubation is extubation occurs prior to 6 hours

    Secondary Outcome Measures

    Total dose of rocuronium or vecuronium
    The total dose of rocuronium or vecuronium administered during the surgical procedure
    Time period of rocuronium or vecuronium administration
    The total interval over which the total dose of rocuronium or vecuronium is administered

    Full Information

    First Posted
    September 23, 2021
    Last Updated
    February 17, 2022
    Sponsor
    University of Washington
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05246397
    Brief Title
    Sugammadex Titration in Cardiac Surgery Patients
    Official Title
    Sugammadex Titration for Reversal of Rocuronium or Vecuronium in Cardiac Surgery Patients
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    February 25, 2022 (Anticipated)
    Primary Completion Date
    February 1, 2023 (Anticipated)
    Study Completion Date
    February 1, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Washington

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Sugammadex is frequently used to reverse the effects of neuromuscular blocking drugs. The recommended doses are 2 mg/kg or 4 mg/kg depending upon the depth of neuromuscular blockade. Clinical studies and experience have suggested that smaller doses may be effective. The purpose of this observational study is to determine the minimal effective dose of sugammadex by administering 50 mg every 5 minutes until the train-of-four ratio is 0.9 in a cohort of cardiac surgery patients, and to determine the duration of action by measuring the train-of-four every hour for up to 6 hours following reversal.
    Detailed Description
    Neuromuscular blocking drugs are used frequently during general anesthesia. The effects of neuromuscular blocking drugs are measured using a twitch monitor, that stimulates the ulnar nerve and measures the evoked response of the adductor pollicis muscle (thumb flexion), or other intrinsic hand muscle. When a series of 4 twitches is administered, the ratio of the first to the fourth twitch (train-of-four ratio) may be used to gauge the degree of muscle relaxation. A train-of-four ratio of 0.9 or greater is considered to represent adequate recovery from neuromuscular blockade. At the end of surgery, antagonists of neuromuscular blockade are commonly administered to reverse any remaining muscle relaxation. Sugammadex is a highly effective reversal agent of the aminosteroid neuromuscular blockings drugs rocuronium and vecuronium, which are the most commonly used neuromuscular blocking drugs. The recommended dose of sugammadex depends upon the degree of neuromuscular blockade. When at least 1 twitch of the train-of-four is present, the recommended dose of sugammadex is 2 mg/kg. When there are no twitches of the train-of-four present, but at least 1 count of the post tetanic count is present, the recommended dose of sugammadex is 4 mg/kg. However, in several dose ranging studies of sugammadex, and in using sugammadex clinically, we and others have determined that smaller doses of sugammadex, often much less than 2 mg/kg, may be effective producing a train-of-four ratio of 0.9 or greater. Sugammadex binds (encapsulates) aminosteroid neuromuscular blocking drugs tightly and the sugammadex-aminosteroid complex is subsequently cleared by the kidney. Therefore we do not expect that recurrence of neuromuscular blockade would occur, even after small doses of sugammadex, as long as the dose of sugammadex is adequate to produce a train-of-four ratio of 0.9. However, additional studies are needed to confirm that recurrence of neuromuscular blockade does not occur after small doses of sugammadex. The purpose of the proposed study is to test the hypothesis that when sugammadex is titrated in 50 mg increments until the train-of-four ratio is 0.9 or greater, that this train-of-four ratio is maintained and there is no recurrence of neuromuscular blockade. Neuromuscular blockade will be monitored with EMG (electromyography)-based quantitative twitch monitoring (TwitchView). At the end of cardiac surgery, sugammadex will be administered to reverse neuromuscular blockade, as defined by a train-of-four ratio of 0.9 or greater. The patient will then transported asleep, intubated and ventilated to the intensive care unit where the train-of-four ratio of 0.9 or greater will be confirmed on arrival by the respiratory therapist. Instead of administering a standard dose of sugammadex 2 mg/kg or 4 mg/kg, sugammadex will be titrated in 50 mg increments every 5 minutes until a train-of-four ratio of 0.9 or greater is reached. Train-of-four ratio will be measured on arrival in the intensive care unit and then hourly for 6 hours or until extubation if extubation occurs in <6 hours. If the train-of-four ratio is less than 0.9 at any time, additional sugammadex will be administered until the train-of-four ratio is 0.9 or greater. The twitch monitoring results in the operating room just prior to reversal, following reversal and hourly in the intensive care unit will be recorded, along with sugammadex doses. The total dose of rocuronium or vecuronium and the time period of neuromuscular blocking drug will also be recorded. Data will either be recorded in real time by study assistants or retrieved from the electronic medical record. The patient's age, gender, and weight will be recorded.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Coronary Artery Disease, Valvular Heart Disease, Aorta Disease, Heart Failure
    Keywords
    neuromuscular blockade, sugammadex, monitoring, rocuronium, vecuronium

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Cardiac surgery patients
    Arm Type
    Experimental
    Arm Description
    Patients undergoing cardiac surgery
    Intervention Type
    Drug
    Intervention Name(s)
    Sugammadex administration
    Intervention Description
    Sugammadex will be given in 50 mg increments every five minutes for reversal of neuromuscular blockade until reaching a train-of-four ratio of 0.9
    Primary Outcome Measure Information:
    Title
    Total dose of sugammadex required to produce a train-of-four ratio of >0.9
    Description
    Sugammadex will be administered in 50 mg increments every 5 minutes until a train-of-four ratio is reached
    Time Frame
    At the completion of surgery and prior to transport to the intensive care unit. The elapsed time from completion of surgery to arrival in the intensive care unit is 30 min to 1 hour
    Title
    Twitch monitoring result prior to sugammadex administration
    Description
    The result of twitch monitoring prior to sugammadex administrative
    Time Frame
    Immediately prior to sugammadex administration, at the completion of surgery and prior to transport to the intensive care unit. The elapsed time from completion of surgery to arrival in the intensive care unit is 30 min-1hour
    Title
    Duration of action of reversal
    Description
    The train-of-four ratio will be determined upon arrival to the ICU and every hour for 6 hours or until extubation is extubation occurs prior to 6 hours
    Time Frame
    On arrival to the intensive care unit and hourly thereafter for 6 hours or until extubation, whichever occurs first
    Secondary Outcome Measure Information:
    Title
    Total dose of rocuronium or vecuronium
    Description
    The total dose of rocuronium or vecuronium administered during the surgical procedure
    Time Frame
    Intraoperative (From "anesthesia start" until "surgery end" times)
    Title
    Time period of rocuronium or vecuronium administration
    Description
    The total interval over which the total dose of rocuronium or vecuronium is administered
    Time Frame
    Intraoperative (The time period from "anesthesia start" until "surgery end" time)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria All cardiac surgery patients Exclusion Criteria: Allergic or other adverse response to sugammadex
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    T. Andrew Bowdle, MD, PhD
    Phone
    206-979-0477
    Email
    bowdle@uw.edu
    First Name & Middle Initial & Last Name or Official Title & Degree
    Srdjan Jelacic, MD
    Phone
    206 598-3777
    Email
    sjelacic@uw.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    T. Andrew Bowdle, MD, PhD
    Organizational Affiliation
    University of Washington
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    Data will be shared based on the policy of the journal in which the work is published

    Learn more about this trial

    Sugammadex Titration in Cardiac Surgery Patients

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