Intraoperative Lidocaine Infusion vs. Esmolol Infusion for Postoperative Analgesia in Laparoscopic Cholecystectomy
NCT02327923 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 90
Last updated 2018-11-30
Summary
Comparison of intraoperative infusion of lidocaine and esmolol in the postoperative requirement of opioid for postoperative pain management after laparoscopic cholecystectomy to decrease opioid related side effects and enhance postoperative recovery with multimodal analgesia approach.
Conditions
- Gall Stone Disease
Interventions
- DRUG
-
Lidocaine
Lidocaine intravenous 1.5mg/kg IV bolus at the time of induction followed by IV infusion @ 1.5 mg/kg/hr till the last suture.
- DRUG
-
Esmolol
Esmolol intravenous bolus 0.5 mg/kg at the time of induction followed by infusion @ 5-15 microgram/kg/min till the last suture.
- DRUG
-
Inj. Paracetamol 1 gm IV at the time of induction
- DRUG
-
Lidocaine
Inj. Xylocaine 2% 3 ml will be infiltrated in skin in all port sites prior to incision.
- DRUG
-
Propofol
Inj. Propofol 2- 2.5 mg/kg will be given for induction
- DRUG
-
Inj fentanyl 1.5mg/kg will be given at the time of induction.
- DRUG
-
Vecuronium
Inj Vecuronium 0.1mg/kg will be given at induction and for maintenance.
- DRUG
-
Atropine
Inj Atropine 0.4 mg IV will be given for bradycardia (HR \< 50/min)
- DRUG
-
Ephedrine
- DRUG
-
Morphine
- DRUG
-
Ketorolac
- DRUG
-
Ondansetron
- DRUG
-
Bupivacaine
Inj. Bupivacaine 0.25% 10 ml will be infiltrated at incision site after closure.
- DRUG
-
Tramadol
Inj tramadol 50 mg IV will be given on SOS basis in ward.
- DRUG
-
Neostigmine
50 mcg/kg for reversal of residual neuromuscular blockade
- DRUG
-
Glycopyrrolate
10 mcg/kg with neostigmine
Sponsors & Collaborators
-
B.P. Koirala Institute of Health Sciences
lead OTHER
Principal Investigators
-
Asish Subedi, MD · B.P. Koirala Institute of Health Sciences
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-01-31
- Primary Completion
- 2016-02-29
- Completion
- 2016-04-30
Countries
- Nepal
Study Locations
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