Clinical Trials Directory

Trials / Completed

CompletedNCT02318810

Influence of the Neuromuscular Blockade on Mask Ventilation

The Influence of the Neuromuscular Blockade on Mask Ventilation; a Placebo Controlled, Randomized Trial With Three Different Dosages of Rocuronium (0.3 mg/kg, 0.6 mg/kg and 0.9 mg/kg)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
300 (actual)
Sponsor
University of Rostock · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Mask ventilation during induction of anesthesia can be improved by administration of neuromuscular blocking agents (NMBAs). NMBAs are usually administered after testing mask ventilation; however, muscle relaxants may improve mask ventilation and they do not alter mask ventilation. Thus, growing evidence suggests to administer muscle relaxants before testing mask ventilation. We will study different dosages of rocuronium; we assume that higher dosages of rocuronium will improve mask ventilation compared with lower dosages.

Detailed description

Mask ventilation during induction of anesthesia can be improved by administration of neuromuscular blocking agents (NMBAs). NMBAs are usually administered after testing mask ventilation; however, muscle relaxants may improve mask ventilation and they do not alter mask ventilation. Thus, growing evidence suggests to administer muscle relaxants before testing mask ventilation.We will administer rocuronium 0.3 mg/kg, 0.6 mg/kg, 0.9 mg/kg and saline (placebo group) before starting with mask ventilation. We will grade mask ventilation based on various scores before and after rocuronium application. Afterwards patient's tracheas will be intubated. We assess risk factors for difficult mask ventilation. We hypothesize that rocuronium 0.9 mg/kg will be superior to rocuronium 0.3 mg/kg and saline.

Conditions

Interventions

TypeNameDescription
DRUGRocuronium 0.3 mg/kgPatients receive rocuronium 0.3 mg/kg
DRUGRocuronium 0.6 mg/kgPatients receive rocuronium 0.6 mg/kg
DRUGRocuronium 0.9 mg/kgPatients receive rocuronium 0.9 mg/kg
DRUGPlaceboPatients receive saline

Timeline

Start date
2015-03-01
Primary completion
2016-05-01
Completion
2016-05-01
First posted
2014-12-17
Last updated
2016-05-03

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02318810. Inclusion in this directory is not an endorsement.