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

Completed

• Conditions: anesthesie; Anesthesia; Narcosis

• Registration Number: NL-OMON48823
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2020-08-06
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 250

Inclusion Criteria

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

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.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The outcome of the monitor devies</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>None</p><br>