MedPath

effectiveness of ketamine and propofol on prevention of muscle pain caused after the use of succinyl choline during surgeries

Phase 4
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2022/02/040300
Lead Sponsor
Dr Akanksha bharat
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. ASA Grade 1,2

2. Age 18 to 65 years

3. Both males and females

4. elective surgeries under general anesthesia with endotracheal intubation under effects of succinyl choline

5. Surgeries completed within 3 hrs

Exclusion Criteria

1. Patient with contraindication to succinyl choline use like chronic deblitating illness, raised intracranial tension, myopathy, recent burns{ <2years back}

2. Pregnant patients and lactating mothers

3. Patients with severe cardiovascular, liver or renal disease

4. Morbid obesity{BMI >35}

5. Patients with known allergies to the study drug

6. Patients who has received analgesic+ muscle relaxants medication in last 24 hrs

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study and compare following parameters in both the groups <br/ ><br>1. Severity of fasiculations after succinylcholine administration <br/ ><br>2. Incidence of post operative myalgia <br/ ><br>3. Severity of post operative myalgia after 24hours and 48 hoursTimepoint: After induction agent for severity of fasiculations, <br/ ><br>Post operatively 24 and 48 hours
Secondary Outcome Measures
NameTimeMethod
To study and compare haemodynamic parameters (heart rate and mean arterial pressure) in both groupsTimepoint: Intra operetively 0,2,4,6 minute before induction agent, <br/ ><br>Intra operatively 0,5,10 minute after intubation
© Copyright 2025. All Rights Reserved by MedPath