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Management of Neuromuscular Blocking Agents and Their Antagonism

Clinical Practice Survey on the Management of Neuromuscular Blocking Agents and Their Antagonism During General Anesthesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06238219
Acronym
NMBA_periop
Enrollment
3000
Registered
2024-02-02
Start date
2024-04-17
Completion date
2024-12-31
Last updated
2024-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuromuscular Blocking Agents, Neuromuscular Monitoring

Brief summary

Neuromuscular blocking agents (NMBA) are commonly used in clinical practice during general anesthesia to facilitate induction, intubation and surgery. Some studies have shown that their use can be deleterious if not codified. Recent recommendations concerning their use and antagonization were published in 2023. Research hypothesis: Using a single-center, retrospective practice study, we aim to analyze whether the 2023 ASA and ESAIC recommendations are being implemented regarding the use of neuromuscular blocking agents.

Interventions

Administration of any neuromuscular blocking agent for surgery under general anesthesia

Sponsors

Erasme University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- All patients undergoing surgery with use of neuromuscular blocking agents at our institution

Exclusion criteria

\- Incomplete electronic anesthesia record

Design outcomes

Primary

MeasureTime frameDescription
Adherence to ASA and ESAIC guidelines for the use and monitoring of neuromuscular bocking agents (%)10 hoursTrain of four (TOF) ratio and TOF-count, as well as post-tetanic count (PTC) will be extracted from the electronic anesthesia record together with the type, dosage and timing of neuromuscular blocking agents. At intubation, antagonisation and extubation, the use of monitoring, the correct dose for antagonising agents (neostigmine or sugammadex) will be recorded. Concordance with current guidelines from ASA (American society of anaesthesiologists) and ESAIC (European society of anaesthesia and intensive care) will be analysed with a Chi-square test (observed versus expected). The % of adherence to the guidelines will be reported.

Countries

Belgium

Contacts

Primary ContactDenis Schmartz, MD
denis.schmartz@hubruxelles.be+3225553919
Backup ContactAndréa Gardon, MD
andrea.gardon@hubruxelles.be+3225553919

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026