Infantile - Postoperative Residual Curarization - Study — I-PORC  

Neuromuscular Blockade Clinical Trial

Official title: Observational Study to Detect Postoperative Residual Curarization in Infantile Patients

Status Completed

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, ;

Related Conditions & MeSH terms

• Delayed Emergence from Anesthesia
• Neuromuscular Blockade
• Neuromuscular Monitoring
• Postoperative Residual Curarization

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