Clinical Trials Directory

Trials / Completed

CompletedNCT02500225

Comparison the Effects of Etomidate and Sevoflurane During Electroconvulsive Therapy

Ulku Ozgul, Associate Professor, Inonu University, Department of Anesthesiology and Reanimation

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
25 (actual)
Sponsor
Inonu University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study was to investigate the effects of etomidate or sevoflurane used in electroconvulsive therapy (ECT) on duration of seizure, hemodynamic response and recovery profiles.

Detailed description

Twenty-five patients will be a total of 150 ECT treatments in this prospective, double-blinded, crossover study. Each patient will receive either 0.2 mg/kg etomidate (Group 1) or 8% sevoflurane (Group 2) in 100% oxygen at 6 L/min fresh gas flow until loss of consciousness for their initial electroconvulsive therapy session. In subsequent sessions, patients will receive the alternative sevoflurane concentration and then alternated between doses until the sixth session. Muscle paralysis will achieve with 1 mg/kg succinylcholine. Motor (EMG) and electroencephalography seizure duration (EEG), heart rate (HR) and mean arterial pressure (MAP) values, and recovery times will recorde.

Conditions

Interventions

TypeNameDescription
DRUGEtomidate0.2 mg/kg etomidate
DRUGSevoflurane8% Sevoflurane

Timeline

Start date
2017-01-01
Primary completion
2017-02-01
Completion
2017-02-01
First posted
2015-07-16
Last updated
2019-01-23

Source: ClinicalTrials.gov record NCT02500225. Inclusion in this directory is not an endorsement.