Clinical Trials Directory

Trials / Completed

CompletedNCT02454868

Remifentanil Minimum Effective Dose for Children Intubation Without Neuromuscular Blockade

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Brasilia University Hospital · Academic / Other
Sex
All
Age
2 Years – 9 Years
Healthy volunteers
Accepted

Summary

Introduction: remifentanil's optimal dose for children intubation without neuromuscular blockade is unknown. Method: phase IV adaptative trial using Dixon's up-and-down method for modeling remifentanil's dose-response curve for adequate intubation conditions as defined by previous studies.

Detailed description

Introduction: remifentanil's optimal dose for children intubation without neuromuscular blockade is unknown. Method: phase IV adaptative trial using Dixon's up-and-down method for modeling remifentanil's dose-response curve for adequate intubation conditions as defined by previous studies. Remifentanil doses starting from 2mg/kg will be infused before intubation. When a success occurs next patient's dose will be decreased by 0.25mg/kg/h. When a success does not occur the next patient's dose will be increased by 0.25mg/kg/h. Intubation will be considered adequate if patient does not cough, does not move, if vocal cords are open, if larigocsocpic Cormack grade I or II.

Conditions

Interventions

TypeNameDescription
DRUGRemifentanilRemifentanil for intubation without neuromuscular blockade

Timeline

Start date
2016-07-01
Primary completion
2016-07-01
Completion
2016-07-01
First posted
2015-05-27
Last updated
2016-07-19

Source: ClinicalTrials.gov record NCT02454868. Inclusion in this directory is not an endorsement.