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Clinical Trial Summary

The primary object of this study is, to investigate the current procedure of neuromuscular monitoring at a tertiary academic university medical center.


Clinical Trial Description

Residual neuromuscular block is known to be a significant but frequently overlooked complication after the use of neuromuscular blocking agents. Aim of this prospective, observational study is to detect the incidence and severity of residual paralysis at a tertiary academic german university medical center.

Methods:

All infantile patients recieving neuromuscular blocking agents are included over a 12 week observational period. At the end of the operation procedure, directly prior to tracheal extubation a train-of-four ratio was assessed quantitatively by an independet observer using the TOF Watch SX monitor. Data related to patient postoperative outcome were collected in the operating theatre, during the way to the postoperative care unit (PACU) and during the stay in the PACU:

- incidence of residual paralysis

- incidence of aspiration, bronchospasm, laryngospasm, oxygen desaturation, airway obstruction, ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03804346
Study type Observational [Patient Registry]
Source University of Regensburg
Contact
Status Completed
Phase
Start date May 1, 2017
Completion date July 23, 2017

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