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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02239965
Other study ID # JLT-NM3
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2014
Est. completion date March 2015

Study information

Verified date October 2019
Source Herlev Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Monitoring the degree of neuromuscular blockade in general anaesthesia reduces complications and patient discomfort. However, monitoring is not applied consistently by Danish anaesthesia personnel. Surveys show that part of the explanation is that the anaesthetists often experience problems with the equipment used for monitoring, though the problems have not been described in detail.

We hypothesise that the lack of consistent monitoring in general anaesthesia is caused by insecurity in the anaesthesia personnel's set-up and use of the equipment, as well as in interpreting the measurement results.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date March 2015
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- has been working in the field of anaesthesiology for at least 1 year.

Exclusion Criteria:

- none

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Herlev Hospital Herlev

Sponsors (1)

Lead Sponsor Collaborator
Herlev Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Description of the barriers to consistent neuromuscular monitoring, based on a qualitative analysis of focus group interviews with anaesthesiologists and nurse anaesthetists Focus group interviews will collect participants' perspectives and will be analyzed for thoughts, opinions, and feelings in regard to neuromuscular monitoring. Specific problems experienced with the equipment and other possible barriers to the consistent use of monitoring will be described qualitatively. Focus group interviews conducted Sep. - Oct. 2014 (2 months)
Secondary Description of the problems experienced with neuromuscular monitoring in daily clinical practice The problems experienced with neuromuscular monitoring will be described through a qualitative analysis of clinical observations of the personnel's daily use of the monitoring equipment, Clinical observations conducted in Sep. - Oct. 2014 (2 months)
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