European Perioperative Brugada Survey

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04808193

Enrollment

300

Registered

2021-03-22

Start date

2021-03-31

Completion date

2021-12-31

Last updated

2021-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brugada Syndrome

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.

Interventions

OTHERSurvey

Participants will fill in the survey

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

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.

Design outcomes

Primary

Measure	Time frame	Description
Questionnaire about treatments for Brugada patients	1 hour	Number of participants with treatment-related information as assessed by the survey/questionnaire N/A

Countries

Belgium

Contacts

Primary ContactEvelien Vandeurzen

evelien.vandeurzen@uzbrussel.be192 92 37

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026