Skip to content

Comparison between two different pain relief techniques in patient undergoing laparoscopic nephrectomy

Ultrasound guided anterior quadratus lumborum block at the L2 level versus retro laminar block for analgesia in patient undergoing laparoscopic nephrectomy - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/069862
Enrollment
63
Registered
2024-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Group 1- Quadratus Lumborum block: After induction with General Anaesthesia.Patients will be placed in the lateral decubitus position with the surgical side upward. Quadratus lumborum b

Sponsors

Himalayan Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Type of laparoscopic surgery- Laparoscopic Nephrectomy 2. American Society of Anesthesiologist (ASA) physical status Grade I and II

Exclusion criteria

Exclusion criteria: 1. Known allergies to Local anesthetics. 2. Bleeding disorders 3. Infection at local site 4. Severe Liver and kidney disfunction 5. BMI above 30 kg/m2 6. Inability to give informed consent 7. Psychiatric Disorder

Design outcomes

Primary

MeasureTime frame
To evaluate post operative analgesic effect of ultrasound guided Quadratus lumborum block and ultrasound guided retro laminar block using NRS pain scoring systemTimepoint: To study total Tramadol consumption over 24 hrs and to study pain intensity at 0,30 mins,2,4,6,8,12,18 and 24 hrs interval respectively

Secondary

MeasureTime frame
1. Total opioid consumption over 24 hours 2. Time of first analgesic used over 24 hours ( time from PACU discharge To first requested analgesic) 3. Patient satisfaction using a Likert-scale questionnaire on POD-1 · Any opioid related side effects like respiratory depression, pruritis within the first 24 hours.Timepoint: Preoperatively (baseline), immediately after block 0.5,10,15,20,25,30, during induction and intubation, intraoperatively at 5,10,15,20,25,30,45,60,75,90,105,120 mins and postoperatively at 0,15,30 mins, 1,2,3,4,6,8,10,12,16,20 and 24 hrs interval respectively.

Countries

India

Contacts

Public ContactDr Amrit Bhardwaj

Himalayan institute of medical sciences

amritmicu@gmail.com8802012126

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026