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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04559386
Other study ID # EUNeuroMuscMonitoringSurvey3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 10, 2021
Est. completion date March 10, 2022

Study information

Verified date March 2021
Source Universitair Ziekenhuis Brussel
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This survey aims to better define Anesthesiologist's perceived usability of existing anesthesia Neuromuscular Monitoring devices.


Description:

This study consists of a simple online survey that takes approximately 2 minutes to complete. The study aims to assess Anesthesiologist's perceived usability of the different types of anesthesia neuromuscular monitoring devices (quantitative and qualitative). The survey is targeted to individual anesthesiologists, independetly of their degree of experience.


Recruitment information / eligibility

Status Completed
Enrollment 692
Est. completion date March 10, 2022
Est. primary completion date March 10, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Active Anesthesiology department heads of European Anesthesiology departments. Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Survey
Questionnaire

Locations

Country Name City State
Belgium UZ Brussel Jette Brussel

Sponsors (1)

Lead Sponsor Collaborator
Universitair Ziekenhuis Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Usability Is there a use for Neuromuscular monitoring applications in their department? - questionnaire 4 months