Clinical Trials Directory

Trials / Completed

CompletedNCT03065309

Determination of Remifentanil's ED50 for Rapid Sequence Intubation Avoiding Bradycardia and Hypotension in Adults

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Brasilia University Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study will find the median effective dose of remifentanil for rapid sequence intubation which avoids bradycardia and hypotension

Detailed description

Remifentanil is becoming popular for rapid sequence intubation because it has a fast onset and ultra-short half-life. Remifentanil a potent opioid associated to bradycardia and hypotension at high doses.

Conditions

Interventions

TypeNameDescription
DRUGRemifentanilbolus dose

Timeline

Start date
2017-02-25
Primary completion
2017-02-28
Completion
2017-03-01
First posted
2017-02-27
Last updated
2017-09-13

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT03065309. Inclusion in this directory is not an endorsement.