A clinical trial to study effect of Transversus abdominis plane block preoperatively versus postoperatively in patients undergoing laparoscopic surgeries

Not yet recruiting

• Conditions: Medical and Surgical,

• Registration Number: CTRI/2021/12/038974
• Lead Sponsor: Dr Bhanushree G

Brief Summary

Transversus Abdominis Plane (TAP) block produces moreeffective postoperative analgesia and significantly reduces consumption ofpostoperative opioids after various abdominal surgeries. It can be performedeither preoperatively or postoperatively. Furthermore, studies investigatingthe ideal period for TAP block administration are few.

The objective of our study was to investigate, whichperiod is more effective for administration of TAP block on perioperativehemodynamic and postoperative analgesia in patients undergoing laparoscopicabdominal surgeries.

it will be conducted among patients undergoing elective laparoscopic surgeries will be divided into 2 groups of 40 each.

After General anaesthesia 1 group will recieve TAP block before incision and other group 2 will recieve TAP block after surgery. Inj Bupivacaine 0.25% 20ml on each side of abdomen.

perioperative hemodynamic status and post opreative analgesic requirement will be noted along with any adverse side effects

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2021-12-28
• Study Start: 2022-10-01

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Patients giving informed written consent ASA class I and II Patients posted for elective Laparoscopic abdominal surgeries.

Exclusion Criteria

patient who refused to give informed written consent Emergency surgeries Allergy for local anaesthetics and confirmed local anaesthesia toxicity.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Peri-operative Hemodynamic status	Baseline, 5min, 10min, during incision, during pneumoperitoneum, 15min, 30min, 1hr, 1hr 30 min, 2 hr

Secondary Outcome Measures

Name	Time	Method
duration of analgesia and post-operative analgesic requirement	post extubation, 5 min, 10 min, 15 min, 30 min, 1 hour, 2 hour, 4 hour, 6 hour, 12 hour and 24 hour

Trial Locations

Locations (1)

Bangalore medical college and Research Institute; 🇮🇳 Bangalore, KARNATAKA, India

Bangalore medical college and Research Institute

🇮🇳Bangalore, KARNATAKA, India

Dr Bhanushree G

Principal investigator

7975398842

bhanuguddi@gmail.com