To evaluate the analgesic efficacy of transmuscular quadratus lumborum block in percutaneous nephrolithotomy

Recruiting

Conditions: Urinary calculus, unspecified,

Registration Number: CTRI/2022/12/047972

Lead Sponsor: Baraniya Pandirajan

Brief Summary: Randomised double-blinded study- Transmucular quadratus lumborum block QL3(20ml of 0.25% Bupivacaine in Group A,20ml of saline in Group B) in percutaneous nephrolithotomy to measure postoperative requirement of analgesic Inj.Tramadol

Detailed Description: Not available

Recruitment & Eligibility

Status: Open to Recruitment

Sex: All

Target Recruitment: 66

Inclusion Criteria

Patient age >18yrs ASA status 1,2 Elective percutaneous nephrolithotomy.

Exclusion Criteria

Refusal to participate in the study Age <18yrs ASA 4 & 5 Known coagulation disorder Allergy to local Anaesthetics Unconscious or mentally incompetent Pregnancy & hemodynamic instability.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare 2 groups,	0h(immediate post extubation);15min,1h,2h,4h,6h,8h,14h,20h,24h
Cumulative tramadol consumption.	0h(immediate post extubation);15min,1h,2h,4h,6h,8h,14h,20h,24h

Secondary Outcome Measures

Name	Time	Method
Assessing theanalgesic efficacy of quadratus lumborum block postoperatively	Assessing theanalgesic efficacy of quadratus lumborum block postoperatively at 15mins,1hr,2hr in PACU and every 2nd hourly for 8hr and every 6th hourly for 24hours
to observe the changes in hemodynamic parameters intraoperatively such as heart rate,systolic and diastolic blood pressure

Trial Locations

Locations (1): Sri Ramachandra institute of higher education and research
🇮🇳
Kancheepuram, TAMIL NADU, India
Sri Ramachandra institute of higher education and research
🇮🇳Kancheepuram, TAMIL NADU, India
Baraniya
Principal investigator
9952994875
baru231995@gmail.com