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comparision of Dexmedetomidine and Thiopental with ?Dexmedetomidine and Ketamin on hemodynamic response ?and duration of seizure in patients candidated for ECT

Phase 2
Recruiting
Conditions
Electroconvulsive therapy.
Registration Number
IRCT20141209020258N81
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
104
Inclusion Criteria

no addiction

Exclusion Criteria

Seizures are less than 25 seconds or they may have arrhythmias or hemodynamic threats during the ECT

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of recovery. Timepoint: fisrt and end of recovery. Method of measurement: minute.;Duration of seizure after entering recovery. Timepoint: start and end of seizure. Method of measurement: minute.;Blood pressure. Timepoint: Before and after ECT and recovery. Method of measurement: Barometer.;Heart rate. Timepoint: Before and after ECT and recovery. Method of measurement: Beats in minutes.;Duration of seizure. Timepoint: Start and end of seizure. Method of measurement: Minute.
Secondary Outcome Measures
NameTimeMethod
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