To determine whether Perfusion index can be used as a measurement in pain management during laparoscopic surgeries under general anaesthesia
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063766
- Lead Sponsor
- Seth GSMC and KEMH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA class l and class ll
Planned for laparoscopic surgeries under general anesthesia.
Exclusion Criteria
Patients refusing to participate in the study
Pregnant females
Neurological and psychiatric diseases
Chronic pain disorders,peripheral vascular disorders,ischaemic hearts disorders.
Autonomic dysfunction or drugs affecting the autonomic system.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare changes in the perfusion index to pain stimulus (1st laparoscopic port insertion) & its variability to subsequent pain stimuli (2nd, 3rd & 4th laparoscopic port insertions) after intravenous administration of analgesic dose of fentanyl.Timepoint: 1st laparoscopic port insertion <br/ ><br>2nd laparoscopic port insertion <br/ ><br>3rd laparoscopic port insertion <br/ ><br>Every minute up to first 10 minutes followed by every five minutes up to 30 minutes
- Secondary Outcome Measures
Name Time Method To compare corresponding changes in perfusion index with dynamic parameters like pulse rate, non invasive blood pressure, mean arterial pressure & oxygen SaturationTimepoint: 1st ,2nd ,3rd ,4th laparoscopic port insertions <br/ ><br>Every one minute for first 10 minutes. <br/ ><br>Every five minutes thereafter for next 30 minutes