Clinical Trials Directory

Trials / Completed

CompletedNCT00248729

Effectiveness and Safety Study of Etomidate Versus Midazolam to Help Place a Breathing Tube Outside of the Hospital.

Etomidate Versus Midazolam for Pre-Hospital Intubation: A Prospective, Randomized Trial

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
St. Luke's Hospital, Pennsylvania · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this study was to compare the utility of etomidate and midazolam in helping patients to relax when there was a need for the placement of a ventilation tube by medics who were transporting patients to a hospital in an ambulance.

Detailed description

Study Objective: The objective of this study was to compare the utility of etomidate and midazolam for sedative facilitated intubation (SFI), without paralytics, in pre-hospital adult patients. Methods: This prospective, double-blind, randomized trial was conducted with two ground pre-hospital Advanced Life Support (ALS) units. All patients age 18 or over transported by the two participating systems requiring pre-hospital SFI were eligible for participation. The ambulances were stocked with blinded numbered syringes, each containing either 7mg of midazolam or 20mg of etomidate. Contact with the Medic Command physician was not required and no paralytics were used. If sedation was not achieved with the study drug, medics could request additional sedation from a Medical command physician; only midazolam or diazepam were available outside of the study.

Conditions

Interventions

TypeNameDescription
DRUGEtomidate (20mg) or Midazolam (7mg)

Timeline

Start date
2002-10-01
Completion
2005-11-01
First posted
2005-11-04
Last updated
2025-05-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00248729. Inclusion in this directory is not an endorsement.