To observe the effect of applying acupressure to different points on the starting dose of Propofol while giving anesthesia.
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056395
- Lead Sponsor
- SGPGIMS LUCKNOW
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients of either sex, aged 18-65 years with American Society Anaesthesiologists’ physical status I- II.
2.Scheduled for elective surgical procedures requiring general anaesthesia with propofol as an induction agent will be enrolled in the study.
Exclusion Criteria
1.Patient’s refusal
2.Patient unable to understand the acupressure technique
3.Allergy to propofol
4.History of cardiac, cerebrovascular, respiratory, hepatic, or renal diseases
5.Predicted difficult airway
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total induction dose of propofol for general anaesthesiaTimepoint: One time
- Secondary Outcome Measures
Name Time Method 1. Total intraoperative propofol requirement <br/ ><br>2. Intraoperative awareness <br/ ><br>3. Postoperative nausea & vomitingTimepoint: 1. One time at the end of anesthesia-Total intraoperative propofol requirement <br/ ><br>2. One time 4 hour after the surgery-Intraoperative awareness <br/ ><br>3. On time after 24 hours of surgery -Postoperative nausea & vomiting