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Evaluation of the TOF CUFF for perioperative neuromuscular transmission monitoring during recovery of moderate and deep neuromuscular block compared to acceleromyography and electromygraphy

Evaluation of the TOF CUFF for perioperative neuromuscular transmission monitoring during recovery of moderate and deep neuromuscular block compared to acceleromyography and electromygraphy - To CUFF

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48823
Enrollment
250
Registered
2019-07-22
Start date
2017-11-17
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

anesthesie Anesthesia Narcosis

Interventions

anesthesia
monitoring
relaxation

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: (i) ASA class I-III (ii) > 18 years of age; (iii) Ability to give oral and written informed consent.

Exclusion criteria

Exclusion criteria: (i) Known or suspected neuromuscular disorders impairing neuromuscular function; (ii) Allergies to muscle relaxants, anesthetics or narcotics; (iii) A (family) history of malignant hyperthermia; (iv) Women who are or may be pregnant or are currently breast feeding; (v) Renal insufficiency, as defined by a glomerular filtration rate

Design outcomes

Primary

MeasureTime frame
The outcome of the monitor devies

Secondary

MeasureTime frame
None

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)