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Comparison of two drugs in psychiatric patients planned for electroconvulsive therapy.

Not Applicable
Conditions
Health Condition 1: O- Medical and SurgicalHealth Condition 2: G- Mental HealthHealth Condition 3: F060- Psychotic disorder with hallucinations due to known physiological condition
Registration Number
CTRI/2024/07/070128
Lead Sponsor
Department of anesthesiology and pain medicine Pt JNM Medical College Raipur
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patient who will give consent by himself or legally authorized representative will be included in study

ASA grade 1 and 2

BMI less than 30

Exclusion Criteria

Pregnancy

Major cardiac issues - Ischemic heart disease, Heart blocks, arrhythmia,

Patient with increased intra-cranial pressure.

Patient with respiratory diseases – asthma, COPD, chronic bronchitis

Patient on ß-adrenergic blockers and TCA

Known or a family history of adverse reactions to dexmedetomidine or clonidine

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence of agitation in patients after electroconvulsive therapy.Timepoint: 60 minutes <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Change in hemodynamic parameters like heart rate blood pressure <br/ ><br> <br/ ><br>Record the Side effects & complications -respiratory depression hypoxemia bradycardia tachycardia hypotension hypertension sedation delayed recoveryTimepoint: 1 hour
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