Discussion on improving neuromuscular monitoring in anesthesia
International Focus Group-based Discussion on Factors Facilitating an Increased Adoption of Neuromuscular Monitoring.
This study talks to anesthesiologists to see what helps or hinders the use of neuromuscular monitoring tools in anesthesia to improve patient care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 16 (estimated) |
| Sex | All |
| Sponsor | Universitair Ziekenhuis Brussel Academic / other |
| Locations | 1 site (Brugge, WV) |
| Trial ID | NCT06945341 on ClinicalTrials.gov |
What this trial studies
This observational study involves focus group discussions aimed at understanding the factors influencing the adoption of neuromuscular monitoring in anesthesia across different countries. By gathering insights from active anesthesiologists, the study seeks to identify barriers and facilitators to the use of monitoring devices in clinical practice. The findings may help inform strategies to enhance the implementation of these technologies in perioperative care.
Who should consider this trial
Good fit: Ideal candidates for this study are active anesthesiologists practicing in the European Union.
Not a fit: Patients who are not involved in anesthesia or do not have access to neuromuscular monitoring may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved patient safety and outcomes through better neuromuscular monitoring practices in anesthesia.
How similar studies have performed: While there may be limited direct precedents, discussions and focus groups in similar medical fields have shown potential for improving clinical practices.
Eligibility criteria
Show full inclusion / exclusion criteria
Active EU Anaesthesiologists
Where this trial is running
Brugge, WV
- AZ Sint Jan — Brugge, Wv, Belgium (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.