To Cuff Study

Evaluation of the TOF CUFF for perioperative neuromuscular transmission monitoring during recovery of moderate and deep neuromuscular block compared to acceleromyography and electromyography – TO CUFF study

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON24381

Enrollment

250

Registered

2019-06-28

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

N.A.

Interventions

N.A.

Eligibility

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 < 30 ml/min (vi) Scheduled for anesthesia without the use of muscle relaxants.

Design outcomes

Primary

Measure	Time frame
TOF and TOF ratio values differences between both groups	—

Secondary

Measure	Time frame
Time to TOF Ratio 0.9	—

Contacts

Public ContactMaarten Honing

Leids Universitair Medisch Centrum

g.h.m.honing@lumc.nl071529964038

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)