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A Comparative study of Thiopentone Propofol and Propofol–Ketamine mixture for Modified Electroconvulsive Therapy

A comparison of the efficacy of Thiopentone Propofol and mixture of Propofol and Ketamine for Modified Electroconvulsive therapy A double blind randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096815
Enrollment
120
Registered
2025-11-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F322- Major depressive disorder, singleepisode, severe without psychotic features

Interventions

Intervention1: Injection Thiopentone Sodium: Thiopentone Sodium 3 to 5 mg per kg intravenous bolus given as an induction agent before each session of modified electroconvulsive therapy administered as

Sponsors

Pacific Medical College and Hospital Udaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The Patients relative gives consent Adult patients of either sex with an ASA grade of I or II Age range of 18 to 60 years ECT indication- Patients diagnosed with psychiatric conditions for which MECT is indicated.

Exclusion criteria

Exclusion criteria: Patients relative refusal of the MECT procedure Known allergy to the study drug ASA grade more than II History of cardiovascular respiratory or neurological disorders Intracranial lesions or increased intracranial pressure Pregnancy or lactation Epilepsy Neuromuscular disorder

Design outcomes

Primary

MeasureTime frame
To compare the effifacy of Thiopentone, Propofol, and mixture of Propofol and Ketamine on the duration of seizures induced during Modified ECT.Timepoint: To compare the efficacy of Thiopentone, Propofol, and a mixture of Propofol and Ketamine on the duration of seizures induced during Modified ECT at baseline, 1min, 5min, 10min, 15min, 20min

Secondary

MeasureTime frame
Assess hemodynamic parameters like Heart rate, Systolic Blood Pressure, Diastolic Blood Pressure, Mean arterial pressure Agitation score Return of spontaneous ventilationTimepoint: Assess hemodynamic parameters[ Heart rate, Systolic Blood Pressure, Diastolic Blood Pressure, Mean arterial pressure Agitation score Return of spontaneous ventilation at baseline 1 min, 5 min, 10min, 15min, 20min

Countries

India

Contacts

Public ContactDr Rajendra Solanki

Pacific Medical College and Hospital

dr.rajendrasolanki51@gmail.com9414131931

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026