European Perioperative Brugada Survey
Primary Purpose
Brugada Syndrome
Status
Unknown status
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Survey
Sponsored by
About this trial
This is an interventional health services research trial for Brugada Syndrome
Eligibility Criteria
Inclusion Criteria:
- All participants must have received an invitation to participate in the survey through the online platform of the European Society of Anaesthesiology and Intensive Care.
Exclusion Criteria:
- Uninvited participation in the survey is not possible.
Sites / Locations
- UZ BrusselRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Brugada Survey
Arm Description
Survey will be answered by all participants
Outcomes
Primary Outcome Measures
Questionnaire about treatments for Brugada patients
Number of participants with treatment-related information as assessed by the survey/questionnaire N/A
Secondary Outcome Measures
Full Information
NCT ID
NCT04808193
First Posted
February 12, 2021
Last Updated
November 3, 2021
Sponsor
Universitair Ziekenhuis Brussel
1. Study Identification
Unique Protocol Identification Number
NCT04808193
Brief Title
European Perioperative Brugada Survey
Official Title
European Perioperative Brugada Survey
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 31, 2021 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitair Ziekenhuis Brussel
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
The aim of this survey is to assess the current perception and clinical practice of Resident and Board-certified Anaesthesiologists and Intensivists regarding perioperative care of patients burdened with the Brugada Syndrome. It is intended to investigate this primarily on national and secondarily on European level.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brugada Syndrome
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Brugada Survey
Arm Type
Experimental
Arm Description
Survey will be answered by all participants
Intervention Type
Other
Intervention Name(s)
Survey
Intervention Description
Participants will fill in the survey
Primary Outcome Measure Information:
Title
Questionnaire about treatments for Brugada patients
Description
Number of participants with treatment-related information as assessed by the survey/questionnaire N/A
Time Frame
1 hour
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
All participants must have received an invitation to participate in the survey through the online platform of the European Society of Anaesthesiology and Intensive Care.
Exclusion Criteria:
Uninvited participation in the survey is not possible.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Evelien Vandeurzen
Phone
192 92 37
Email
evelien.vandeurzen@uzbrussel.be
Facility Information:
Facility Name
UZ Brussel
City
Jette
State/Province
Brussel
ZIP/Postal Code
1090
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Evelien Vandeurzen, Master
Phone
024749237
Email
evelien.vandeurzen@uzbrussel.be
First Name & Middle Initial & Last Name & Degree
Panagiotis Flamée, MD
First Name & Middle Initial & Last Name & Degree
Hugo Carvalho, MD
First Name & Middle Initial & Last Name & Degree
Jan Poelaert, MD, PhD
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
European Perioperative Brugada Survey
We'll reach out to this number within 24 hrs