Skip to main content
OpenTrials
Completed

NCT Number: NCT02939911

Residual Neuromuscular Blockade in Pediatric Anesthesia

Residual neuromuscular blockade (RNB) is frequent and it is associated with postoperative morbidity and mortality. The incidence of the RNB in pediatric anesthesia is currently not known. The aim of this prospective observational cohort study is to evaluate the early RNB just before extubation and late RNB at the time of arrival to postanesthetic care unit (PACU).

Completed

Looking for future studies?

Notify Me

Key information

Age range

29 week–19 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Brno University Hospital

Brno, 62500, Czechia

About this study

Residual neuromuscular blockade (RNB) is frequent and it is associated with negative impact on postoperative morbidity and mortality. The incidence of the RNB in adult is well described, however in pediatric subpopulation it is currently not known. The aim of this prospective observational cohort study is to evaluate the early RNB just before extubation and late RNB at the time of arrival to postanesthetic care unit (PACU). In the trial will be enrolled all pediatric patients (28 weeks of age and older - 19 years old) whom will be administered neuromuscular blocking agent during anesthesia. The demographic data will be collected including: age, weight, type of surgery, ASA status. The anesthesia management will be described including: airway management, type and cumulative dose of neuromuscular blocking agent (NMBA) and time and dose of the last administered bolus of NMBA. The residual neuromuscular blockade will be measured according to the standards: TOF Watch accelerometry at the moment prior to extubation (two measurements) in TOF mode and at the arrival to postanesthetic care unit (PACU) (two measurements) in TOF mode.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Paediatric patients undergoing surgery with neuromuscular blocking agents were administered with the age limits

Exclusion criteria

  • weight under 3000 grams
  • neuromuscular disease
  • haemodynamic impairment (vasopressor need)
  • planned postoperative mechanical ventilation

Treatment and study plan

Residual neuromuscular blockade measurement

Device

Just prior extubation in OR and at the arrival to PACU the residual neuromuscular blockade will be measured by accelerometry

Other names: accelerometry

Primary outcomes

  1. Early residual neuromuscular blockade

    Time frame: before extubation

    Just prior extubation the residual neuromuscular blockade will be measured by accelerometry

Secondary outcomes

  1. Late neuromuscular blockade

    Time frame: at arrival to PACU

    At the arrival to PACU the residual neuromuscular blockade will be measured by accelerometry

Sponsors and collaborators

Lead sponsor

Brno University Hospital

Other

Registry information

Official study title

Residual Neuromuscular Blockade in Paediatric Patients Before Extubation and in Postanesthetic Care Unit:Prospective Observational Cohort Study

Acronym: REPEB

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Oct 20, 2016
Registry last updated
Nov 19, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.