Health Condition 1: null- Inclusion criteria: Scheduled for elective laparoscopic cholecystectomy Patients aged 18-60 years American Society of Anesthesiologists Physical Status I & II
Conditions
Interventions
Intervention1: Propofol-fentanyl group: Induction with injection propofol 1.5mg/kg IV and maintenance with 3-12mg/kg/h propofol infusion along with fentanyl infusion at rate of 1mcg/kg/hr.
Control In
Sponsors
DirectorSri Venkateswara Institute of Medical Sciences
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: Scheduled for elective laparoscopic cholecystectomy Ppatients aged 18-60 years American Society of Anesthesiologists Physical Status I & II15
Exclusion criteria
Exclusion criteria: Exclusion criteria: Chronic opioid users Pre-existing pain syndrome Severe cardiovascular(New York Heart Association class III or IV) Severe pulmonary and renal disease Inability to communicate and understand Pain scale(Visual analogue scale) Pregnant and lactating mothers Patients not willing to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Primary objective is to find out the incidence of chronic post-operative surgical pain(CPSP) after laparoscopic cholecystectomyTimepoint: At 1st,2nd,3rd and 4th months after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| 2. Secondary objective is to compare the (1)incidence of CPSP and (2)recovery profile between two different types of TIVA.Timepoint: (1)1st ,2nd ,3 rd and 4th month after laparoscopic cholecystectomy (2)Post operative period (time frame 0-24h) | — |
Countries
India
Contacts
Public ContactDr Aloka Samantaray
Department of Anaesthesiology& Critical Care Sri Venkateswara Institute of Medical Sciences Tirupati
Outcome results
None listed