A Comparative Evaluation Of Propofol Versus Dexmedetomidine Effects On Haemodynamic Responses, Seizure Duration And Recovery Profile Following Electroconvulsive Therapy

Not Applicable

Not yet recruiting

• Conditions: Mental and Behavioural Disorders; Anaesthesia

• Registration Number: PACTR202402621085427
• Lead Sponsor: SELF FUNDED

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-02-04
• Last Update Posted: 4 March 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 76

Inclusion Criteria

1.Age 18 years and above.
2.Patients with American Society of Anesthesiologists (ASA) physical status class I or II.

Exclusion Criteria

1.Refusal of Patient or guardian to give written informed consent.
2.Age below 18 years.
3.Patient with ASA > II
4.History of allergy or sensitivity to the study medications.
5.Presence or evidence of raised intracranial pressure.
6.Presence of glaucoma
7.Present or recent myocardial infarction (by history or ECG, lab results).
8.Anticipated difficult airway
9.Systemic hypertension

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Mean arterial pressure changes at 1 min

Secondary Outcome Measures

Name	Time	Method
1. Haemodynamic changes at 1 min, 5 min, 10 min and 20 min.<br>2. Seizure duration<br>3. Recovery time<br>4. Post-ECT pain score using Pain Assessment in Advanced Dementia (PAINAD) scale<br>