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
| Type | Name | Description |
|---|---|---|
| DRUG | Etomidate | 0.2 mg/kg etomidate |
| DRUG | Sevoflurane | 8% 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.