Study Evaluating the Efficacy & Safety of Remifentanil in a Rapid Sequence

Clinical Trial Summary

The primary objective is to determine whether, during a rapid sequence intubation by etomidate, and succinylcholine Sellick maneuver, the administration of remifentanil at 2 different dosages (0.5 and 1.0 microgram per kg body weight), reduces potentially dangerous reactional tachycardia.

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NCT number	NCT01259648
Study type	Interventional
Source	Centre Hospitalier Universitaire de Nimes
Contact
Status	Completed
Phase	Phase 4
Start date	March 9, 2011
Completion date	May 20, 2014

Study Evaluating the Efficacy and Safety of Remifentanil in a Rapid Sequence Induction for Fragile Subjects

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms