Improving Neuromuscular Monitoring and Reducing Residual Neuromuscular Blockade Via E-learning

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

6525 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-11-21

Study Completion Date

2017-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To assess the impact of an e-learning course in neuromuscular monitoring on the frequency of application of objective neuromuscular monitoring for assessment of depth of neuromuscular blockade in general anaesthesia and secondarily on the incidence of residual neuromuscular blockade after anesthesia.

We will collect data prospectively from 6 Danish anaesthesia departments from the time of intervention, using data from the Anaesthesia Information Management System (AIMS). Baseline data is obtained from another study based on the same data extraction procedure (NCT02914119).

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Development and Validation of an Android-based Application for Anaesthesia Neuromuscular Monitoring

NCT03605225

Neuromuscular Blockade Neuromuscular Monitoring

COMPLETED NA

Neuromuscular Blockade Monitoring Using Kine-myography vs Electromyography.

NCT05992090

Neuromuscular Blockade Residual Neuromuscular Blockade

COMPLETED

Algorithm of Muscle Function Tests to Detect Residual Neuromuscular Blockade.

NCT03219138

Postoperative Residual Curarization

COMPLETED NA

OS NMB Depth Measured by Central and Peripheral Monitor.

NCT03660891

Neuromuscular Blockade

UNKNOWN

Incidence of Incomplete Postoperative Neuromuscular Recovery From Anesthesia (P07535)(Completed)

NCT01181349

Neuromuscular Blockade

COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Neuromuscular Blockade

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

E-learning course

Group Type EXPERIMENTAL

E-learning course in neuromuscular monitoring

Intervention Type OTHER

An e-learning course designed to assess the challenges and common problems experienced by anesthetists when monitoring the neuromuscular blockade during general anesthesia.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

E-learning course in neuromuscular monitoring

An e-learning course designed to assess the challenges and common problems experienced by anesthetists when monitoring the neuromuscular blockade during general anesthesia.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Anaesthetists We will include the following anaesthesia personnel as anaesthetists: nurse anaesthetists in training, nurse anaesthetists, first year residents in anaesthesiology, residents in the last 4 years of training in anaesthesiology, and specialist consultants in anaesthesia.

Patients We will include and collect data from all patients undergoing general anaesthesia with neuromuscular blockade in each data collection period. Patients, who are eligible more than once, i.e. undergoing general anaesthesia on more than one occasion, will be included in the analyses with a case for every general anaesthetic received.

Eligible Sex

ALL

Accepts Healthy Volunteers

No