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Comparison of Intraoperative Intravenous Lidocaine Infusion and Transversus Abdominis Plane (TAP) Block for Post-operative Analgesia Following Laproscopic Cholecystectomy

A

Aga Khan University Hospital, Pakistan

Status

Completed

Conditions

Post Operative Pain

Treatments

Drug: Lidocaine IV
Drug: Ropivacaine

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study is aimed to determine the post operative pain after laparoscopic cholecystectomy by dividing patients into three different group. Group A will receive lidocaine 2mg/kg bolus at induction followed by 1.5mg/kg/hr infusion. Group B will receive bilateral subcostal TAP block with 0.375% 20ml Ropivicaine on each side. Group C will not receive any additional pain regime apart from the routine intraoperative analgesics. Pain score will be assessed post operatively for 24 hours at regular intervals using visual analog score.

Enrollment

90 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age group (18-65)
  • Undergoing elective Laproscopic Cholecystectomy
  • ASA status I or II

Exclusion criteria

  • Participation in any other trial
  • Known hypersensitivity to study medications
  • Chronic Opioid used
  • Seizure disorder

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

90 participants in 3 patient groups

Lidocaine Group
Experimental group
Description:
After induction of anaesthesia, a bolus of 2mg/kg intravenous lidocaine will be given followed by Lidocaine infusion at the rate of 1.5 mg/kg/hour which will be stopped at the end of surgery.
Treatment:
Drug: Lidocaine IV
TAP group
Experimental group
Description:
After completion of procedure and before extubation, bilateral ultrasound guided subcoastal transversus abdominis plane (TAP) block will be performed by the primary anaesthetist. After taking aseptic measures, with patient in supine position a high frequency (6-13 MHz) linear ultrasound probe will be placed obliquely just inferior to the costal margin over the anterior abdominal wall. With the help of a 21G or 22G, 100 mm needle, 20 ml of 0.375% Ropivacaine will be injected between rectus sheath and fascia of transversus abdominis muscle, bilaterally.
Treatment:
Drug: Ropivacaine
Control group
No Intervention group
Description:
No additional intervention will be given to this group

Trial contacts and locations

1

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Central trial contact

Haris Sheikh, MBBS; Hameed Ullah, FCPS

Data sourced from clinicaltrials.gov

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