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Better pretreatment agent to reduce pain associated with propofol injection pain between ketamine vs lidocaine injection at the time of induction of general anaesthesia during surgical procedures

Phase 3
Conditions
Health Condition 1: K800- Calculus of gallbladder with acutecholecystitisHealth Condition 2: K566- Other and unspecified intestinal obstruction
Registration Number
CTRI/2023/09/057987
Lead Sponsor
Sms medical college jaipur
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients willing to participate in the study

2.Patients with age between 18 years to 55 years.

3.American Society of Anaesthesiologist (ASA) Grade I and II.

4.Undergoing elective urological, Gynaecological or general surgical procedures.

5.Patients undergoing routine elective surgical procedures under General anaesthesia

Exclusion Criteria

1.Patients not willing to participate in study

2.Patients with history of known hypersensitivity to Propofol injectable emulsion or any of its components.

3.Pregnant women.

4.Nursing mothers.

5.Morbid obesity (BMI >35).

6.Chronic steroid use.

7.Patients on antidepressants or opioid dependence or suffering from any psychiatric disease

8.Patients with chronic pain (arthritis, malignancies).

9.Those having difficulty in venous access

10.Uncontrolled hypertension

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence & severity of pain of propofol injection with a verbal response & behavioural signs such as facial grimacing,arm withdrawal or tears at different time intervals <br/ ><br>0 seconds <br/ ><br>1 minutes <br/ ><br>2 minutesTimepoint: 2 minutes
Secondary Outcome Measures
NameTimeMethod
Hemodynamic variables <br/ ><br>1 HR <br/ ><br>2 SBP <br/ ><br>3 DBP <br/ ><br>4 SpO2Timepoint: 20 minutes
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