Recovery of patients after sleep dose of Propofol vs Dexmedetomidine

Not Applicable

Completed

• Conditions: Health Condition 1: null- ASA1 and 2

• Registration Number: CTRI/2017/09/009795
• Lead Sponsor: Mahatma Gandhi medical college and research institute

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2017-12-27
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 40

Inclusion Criteria

Patients ASA1 and 2 scheduled for elective short day care gynaecological surgery duration < 30Min under Iv sedation

Exclusion Criteria

Patients with known allergies to any of the test drugs,pregnancy,Drug abuse,chronic pain condition,Difficult airway, BMI > 35,Neurological disorder,psychological disorder

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Modified Aldrete score,Finger Taper Test,Visual spatial memory Test,Timepoint: Modified Aldrete score every 1 min till score 9-10,Finger Taper Test and Visual spatial memory Test every hour till 4 hour

Secondary Outcome Measures

Name	Time	Method
Heart rate, mean arterial blood pressure,Respiratory Rate and SpO2,Sedation score <br/ ><br>Timepoint: Heart rate, mean arterial blood pressure,RR and SpO2 (Baseline,Every two minute for 10 minutes,Then every 5 minutes until the end of surgery) <br/ ><br>Sedation scores assessment <br/ ><br>(Every two minute for 10 minutes,Then every 5 minutes until the end of surgery) <br/ ><br>