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
About this trial
This is an interventional other trial for Coronary Artery Disease focused on measuring neuromuscular blockade, sugammadex, monitoring, rocuronium, vecuronium
Eligibility Criteria
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
NCT ID
NCT05246397
First Posted
September 23, 2021
Last Updated
February 17, 2022
Sponsor
University of Washington
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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