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OpenTrials
Completed

NCT Number: NCT04564404

Neuromusculaire Monitoring Survey

This survey aims to better define the willingness-to-buy for Applications in Neuromuscular Monitoring throughout European hospitals.

Completed

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Key information

Conditions

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UZ Brussel

Jette, Brussels Capital, 1090, Belgium

About this study

This study consists of a simple online survey that takes approximately 2 minutes to complete.

The study aims to assess the willingness-to-buy for Applications in Neuromuscular Monitoring (monitoring and software-based) within the anesthesia departments of European hospitals. The survey is targeted to the department heads of the questioned anesthesia departments.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Active Anesthesiology department heads of European Anesthesiology departments.

Exclusion criteria

  • None

Treatment and study plan

Survey

Other

Questionnaire to ask about the willingness-to-buy applications in neuromuscular monitoring.

Primary outcomes

  1. Willingness to buy questionnaire

    Time frame: 4 months

    Would this person be willing to buy neuromuscular monitoring applications.

Sponsors and collaborators

Lead sponsor

Universitair Ziekenhuis Brussel

Other

Registry information

Official study title

Neuromusculaire Monitoring Survey - Financial

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Sep 25, 2020
Registry last updated
Nov 3, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.