Availability of the Different Types of Anesthesia Neuromuscular Monitoring Devices Throughout European HospitalsNCT04517578
European Neuromuscular Monitoring Survey
An observational study of Availability of the Different Types of Anesthesia Neuromuscular Monitoring Devices Throughout European Hospitals and Health Care Utilization, run by Universitair Ziekenhuis Brussel at 1 site in Belgium.
Trial summary
This survey aims to better define the availability of the different types of anesthesia neuromuscular monitoring devices throughout European hospitals. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Availability of the Different Types of Anesthesia Neuromuscular Monitoring Devices Throughout European Hospitals, Health Care Utilization, Medical Device Availability
- What is being tested?
- Survey
- How many people
- 692 participants
- Where
- 1 siteBelgium
- Study dates
- 10 Nov 2021to 10 Mar 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: anaesthesia departments within the European health system.
Who may be able to join
- Active Anesthesiology department heads of European Anesthesiology departments.
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
Belgium1 site
Universitair Ziekenhuis Brussel
Brussels, Brussels Capital, 1090
About this study
This survey aims to better define the availability of the different types of anesthesia neuromuscular monitoring devices throughout European hospitals.
- Conditions
- Availability of the Different Types of Anesthesia Neuromuscular Monitoring Devices Throughout European Hospitals, Health Care Utilization, Medical Device Availability, Medical Staff Availability
- Being tested
- Survey
- Medical subject headings
- Patient Acceptance of Health Care
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SurveyOther
Participants will be asked to fill in an online survey that will be anonimized.
What is being measured
The primary outcome is the main question the study is designed to answer.
Questionnaire about medical equipment and staff availability
Questionnaire about all medical equipment and staff that is available site per site and what is mainly used.
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Aug 2020
- Study start10 Nov 2021
- Primary completion10 Mar 2022
- Study completion10 Mar 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Availability of the Different Types of Anesthesia Neuromuscular Monitoring Devices Throughout European HospitalsStudies of the same condition, open and under way.
- More trials run by Universitair Ziekenhuis BrusselThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 692 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universitair Ziekenhuis Brussel
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04517578
- Sponsor's protocol ID
- EUNeuroMuscMonitoringSurvey
- Status last verified
- Jul 2021
- First submitted
- 10 Aug 2020
- Last updated
- 3 Nov 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Publication in a journal.
Study at a glance
From the registry record, last updated by the sponsor on 3 Nov 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- European Neuromuscular Monitoring Survey
- ClinicalTrials.gov ID
- NCT04517578
- Acronym / sponsor ID
- EUNeuroMuscMonitoringSurvey
- Conditions
- Availability of the Different Types of Anesthesia Neuromuscular Monitoring Devices Throughout European Hospitals, Health Care Utilization, Medical Device Availability, Medical Staff Availability
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 692 participants (actual)
- Lead sponsor
- Universitair Ziekenhuis BrusselUniversity, hospital or other
- Study start
- 10 Nov 2021 (actual)
- Primary completion
- 10 Mar 2022 (actual)
- Study completion
- 10 Mar 2022 (actual)
- First posted
- 18 Aug 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This survey aims to better define the availability of the different types of anesthesia neuromuscular monitoring devices throughout European hospitals.
Study design
- Observational model
- Other
- Time perspective
- Prospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- anaesthesia departments within the European health system.
Key inclusion criteria (1 listed)
- Active Anesthesiology department heads of European Anesthesiology departments.
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| SurveyParticipants will be asked to fill in an online survey that will be anonimized. | Other | – |
Primary outcome
Questionnaire about medical equipment and staff availability
Time frame: 1 year
Questionnaire about all medical equipment and staff that is available site per site and what is mainly used.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Nov 2022.
- Individual participant dataSharing planned: Yes. Publication in a journal.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Availability of the Different Types of Anesthesia Neuromuscular Monitoring Devices Throughout European Hospitals and Health Care Utilization, run by Universitair Ziekenhuis Brussel at 1 site in Belgium.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 3 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Questionnaire about medical equipment and staff availability (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Nov 2022; AzTrials last refreshed its copy on 8 Nov 2026.