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Benzodiazepine-free Cardiac Anesthesia for Reduction of Postoperative Delirium (B-Free)

Primary Purpose

Delirium, Post-cardiac Surgery

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Limited Intraoperative Benzodiazepine
Liberal Intraoperative Benzodiazepine
Sponsored by
Population Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Delirium

Eligibility Criteria

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

Inclusion Criteria:

  • Hospital is a major surgical center with a minimum of 250 cases of cardiac surgery per year.
  • Equipoise by the hospital physicians regarding the use of benzodiazepines during surgery (≥ 95% of hospital cardiac anesthesia group agrees to manage adult patients (age >18 years) as per the benzodiazepine policy in place during a given crossover period).
  • Hospital routinely assesses patients (age >18 years) for postoperative delirium at least once every 12 hours during the initial 72 hours after cardiac surgery as a part of routine clinical care using either the Confusion Assessment Method-ICU (CAM-ICU) or the Intensive Care Delirium Screening Checklist (ICDSC).

Exclusion Criteria:

- Hospital does not meet inclusion criteria

Sites / Locations

  • Washington University School of Medicine
  • Weill Cornell Medicine
  • Mazankowski Alberta Heart Institute
  • Royal Columbian Hospital
  • Vancouver General Hospital
  • St. Paul's Hospital
  • St. Boniface General Hospital
  • Queen Elizabeth II Health Sciences Centre
  • Hamilton Health Sciences, Hamilton General HospitalRecruiting
  • Kingston General Hospital
  • London Health Sciences Centre
  • Sunnybrook Health Sciences Centre
  • St. Michael's Hospital
  • Toronto General Hospital
  • Montreal Heart Institute
  • Jewish General Hospital
  • Hôpital Laval
  • Centre Hospitalier Universitaire de Sherbrooke
  • Regina General Hospital
  • Royal University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Limited Benzodiazepine Policy

Liberal Benzodiazepine Policy

Arm Description

Policy of no routine use of any intraoperative benzodiazepines.

Policy for the administration of benzodiazepine as per clinical guidelines but no lower than 0.03 mg/kg (ideal body weight midazolam equivalent) to all patients undergoing cardiac surgery. Any benzodiazepine may be used.

Outcomes

Primary Outcome Measures

Incidence of Delirium
Delirium assessed up to 72 hours after surgery using standardized and validated delirium scales

Secondary Outcome Measures

Number of Days in ICU after Cardiac Surgery
Length of Stay (LOS) in Intensive Care Unit after Cardiac Surgery
Number of Days in Hospital after Cardiac Surgery
Length of Stay (LOS) in Hospital after Cardiac Surgery
Incidence of In-hospital Mortality
Death from any cause after index cardiac surgery and during the index hospitalization

Full Information

First Posted
April 18, 2019
Last Updated
April 18, 2023
Sponsor
Population Health Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT03928236
Brief Title
Benzodiazepine-free Cardiac Anesthesia for Reduction of Postoperative Delirium
Acronym
B-Free
Official Title
Benzodiazepine-free Cardiac Anesthesia for Reduction of Postoperative Delirium
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 18, 2019 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Population Health Research Institute

4. Oversight

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

5. Study Description

Brief Summary
B-FREE is a pragmatic, multicentre, cluster crossover trial evaluating whether a policy limiting the use of intra-operative benzodiazepine reduces post-operative delirium when compared with a policy of 'ad libitum' administration. The knowledge generated by this study will provide the basis for cardiac anesthesia practice guidelines.
Detailed Description
Delirium, an acute state of confusion, occurs in approximately 1 in 5 adults after open heart surgery. Even though it is a temporary state, patients who experience delirium are at increased risk of serious problems that last after the delirium has resolved. These problems include decreases in thinking, mobility, self-care, and the ability to live independently in a community setting. Patients who experience delirium have longer stays in hospital, are more likely to be discharged to a nursing home, and are more likely to die. Benzodiazepines are a sedative and amnestic medication that may be associated with delirium. As such, benzodiazepines are rarely used for sedation in the intensive care unit after cardiac surgery. However, benzodiazepines continue to be used frequently in the operating room by anesthesiologists during open heart surgery because of their amnestic effects and limited impact on blood pressure. Nevertheless, practice is divided among cardiac anesthesiologists, with some never using benzodiazepines and others using them for nearly all patients. Because the best approach (routine benzodiazepines or restricted benzodiazepines) remains uncertain, we will compare the effect of a hospital policy of intraoperative medication use that includes benzodiazepines to a policy that uses alternative medications and no benzodiazepines on the incidence of delirium after open heart surgery. The findings of the study have the potential to improve the outcomes of tens of thousands of patients around the world and will provide the basis for cardiac anesthesiology practice guidelines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delirium, Post-cardiac Surgery

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Multicenter, cluster-randomized, crossover trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15886 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Limited Benzodiazepine Policy
Arm Type
Experimental
Arm Description
Policy of no routine use of any intraoperative benzodiazepines.
Arm Title
Liberal Benzodiazepine Policy
Arm Type
Active Comparator
Arm Description
Policy for the administration of benzodiazepine as per clinical guidelines but no lower than 0.03 mg/kg (ideal body weight midazolam equivalent) to all patients undergoing cardiac surgery. Any benzodiazepine may be used.
Intervention Type
Other
Intervention Name(s)
Limited Intraoperative Benzodiazepine
Intervention Description
policy for limited use of intraoperative benzodiazepine
Intervention Type
Other
Intervention Name(s)
Liberal Intraoperative Benzodiazepine
Intervention Description
policy for liberal use of intraoperative benzodiazepine
Primary Outcome Measure Information:
Title
Incidence of Delirium
Description
Delirium assessed up to 72 hours after surgery using standardized and validated delirium scales
Time Frame
up to 72 hours post cardiac surgery
Secondary Outcome Measure Information:
Title
Number of Days in ICU after Cardiac Surgery
Description
Length of Stay (LOS) in Intensive Care Unit after Cardiac Surgery
Time Frame
through study completion, approximately 37 months
Title
Number of Days in Hospital after Cardiac Surgery
Description
Length of Stay (LOS) in Hospital after Cardiac Surgery
Time Frame
through study completion, approximately 37 months
Title
Incidence of In-hospital Mortality
Description
Death from any cause after index cardiac surgery and during the index hospitalization
Time Frame
through study completion, approximately 37 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hospital is a major surgical center with a minimum of 250 cases of cardiac surgery per year. Equipoise by the hospital physicians regarding the use of benzodiazepines during surgery (≥ 95% of hospital cardiac anesthesia group agrees to manage adult patients (age >18 years) as per the benzodiazepine policy in place during a given crossover period). Hospital routinely assesses patients (age >18 years) for postoperative delirium at least once every 12 hours during the initial 72 hours after cardiac surgery as a part of routine clinical care using either the Confusion Assessment Method-ICU (CAM-ICU) or the Intensive Care Delirium Screening Checklist (ICDSC). Exclusion Criteria: - Hospital does not meet inclusion criteria
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
B-Free Study Coordinator
Phone
905212100
Email
B-FREE@phri.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jessica Spence, MD FRCPC
Organizational Affiliation
Population Health Research Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eric Jacobsohn, MBChB MPHE
Organizational Affiliation
University of Manitoba
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stuart Connolly, MD FRCPC
Organizational Affiliation
Population Health Research Institute
Official's Role
Study Chair
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110-1010
Country
United States
Individual Site Status
Active, not recruiting
Facility Name
Weill Cornell Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States
Individual Site Status
Active, not recruiting
Facility Name
Mazankowski Alberta Heart Institute
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2B7
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Royal Columbian Hospital
City
New Westminster
State/Province
British Columbia
ZIP/Postal Code
V3L 3W7
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1M9
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
St. Paul's Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6Z 1Y6
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
St. Boniface General Hospital
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R2H 2A6
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Queen Elizabeth II Health Sciences Centre
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 3A7
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Hamilton Health Sciences, Hamilton General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emilie P Belley-Côtê, MD
Phone
905-527-4322
Ext
40306
Email
Emilie.Belley-Cote@phri.ca
First Name & Middle Initial & Last Name & Degree
Richard P Whitlock, MD
Facility Name
Kingston General Hospital
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 2V7
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B 1W8
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Toronto General Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Montreal Heart Institute
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H1T 1C8
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Jewish General Hospital
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H3T 1E2
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Hôpital Laval
City
Québec
State/Province
Quebec
ZIP/Postal Code
G1V 4G5
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Centre Hospitalier Universitaire de Sherbrooke
City
Sherbrooke
State/Province
Quebec
ZIP/Postal Code
J1H 4C6
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Regina General Hospital
City
Regina
State/Province
Saskatchewan
ZIP/Postal Code
S4P 0W5
Country
Canada
Individual Site Status
Active, not recruiting
Facility Name
Royal University Hospital
City
Saskatoon
State/Province
Saskatchewan
ZIP/Postal Code
S7N OW8
Country
Canada
Individual Site Status
Active, not recruiting

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33721875
Citation
Wang ML, Min J, Sands LP, Leung JM; the Perioperative Medicine Research Group. Midazolam Premedication Immediately Before Surgery Is Not Associated With Early Postoperative Delirium. Anesth Analg. 2021 Sep 1;133(3):765-771. doi: 10.1213/ANE.0000000000005482.
Results Reference
derived

Learn more about this trial

Benzodiazepine-free Cardiac Anesthesia for Reduction of Postoperative Delirium

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