Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Total Intravenous Anesthesia using Propofol: After adequate preoxygenation, anesthesia will be induced with i.v propofol with a target control infusion pump using Schneider model target
Sponsors
All India Institute of Medical Sciences
Eligibility
Inclusion criteria
Inclusion criteria: Patients undergoing surgery for Carcinoma Gall Bladder belonging to ASA class I,II and III
Exclusion criteria
Exclusion criteria: 1. Patient refusal 2. Allergy to propofol or any study drugs 3. Chronic kidney or liver disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To detect the difference in post-operative serum TGF-β levels in patients receiving Propofol-based Total Intravenous Anesthesia versus inhalational based anesthesiaTimepoint: Pre-operative and 24 hours after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare incidence of post-operative complicationsTimepoint: up to 24 hours after surgery;To detect difference in peri-operative systemic inflammation and anti-tumor immunity: change between pre-operative and post-operative T-helper cell profile, IL-6, NLR, PLR, MLR and modified Glasgow prognostic scoreTimepoint: Pre-operative and 24 hours after surgery | — |
Countries
India
Contacts
Public ContactAnkit Sharma
Dr BRA IRCH, AIIMS
Outcome results
None listed