Health Condition 1: F319- Bipolar disorder, unspecified Health Condition 2: F28- Other psychotic disorder not due to a substance or known physiological condition Health Condition 3: F259- Schizoaffective disorder, unspecified Health Condition 4: F209- Schizophrenia, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: This study will be conducted on patients suffering from a mental disorder as per ICD 11 and requiring modified electroconvulsive therapy as per the decision of the consultant psychiatrist.
Exclusion criteria
Exclusion criteria: This study will be conducted on the following patients: patients with a history of relevant drug allergy. patients who have had prior treatment with ECT. patients with a history of substance abuse with relevant drugs. patients with anticipated difficult airway.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the seizure duration produced with etomidate to that with propofol in patients undergoing modified ECT. Timepoint: From the time application of stimulus until the subsidence of convulsions, the normal range of convulsions induced being 15-100 seconds | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the effect on haemodynamics produced with Etomidate to that with Propofol in patients undergoing modified ECT, in terms of - 1.Heart rate , 2.Systolic blood pressure (SBP), 3.Diastolic blood pressure (DBP) , 4.Mean arterial pressure (MAP) 5.Oxygen saturation (spo2) and 6. EtCO2 Timepoint: 1.Heart rate 2.Systolic blood pressure 3.Diastolic blood pressure 4.Mean arterial pressure 5.Oxygen saturation (spo2) 6. EtCO2 will be recorded before induction (T0), after administration of study drug(T1), during the seizure activity(T2) & after 1(T3), 3(T4), 5(T5), & 10 min (T6) of seizure activity. | — |
Countries
India
Contacts
NKP Salve institute of medical sciences