FindTrial
Sign In

This is a clinical study to know the effectiveness of quadratus lumborum block in relieving post operative pain of patients undergoing renal transplantation

Efficacy of ultrasound guided quadratus lumborum block as postoperative analgesia in patients undergoing renal transplantation â?? a randomize double blind clinical study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/06/008924
Enrollment
60
Registered
2017-06-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- renal transplant recepients undergoing general anaesthesia

Interventions

Intervention1: Ultrasound guided Quadratus lumborum block: After obtaining institutional ethical committee (IEC) clearance, patients will be randomized into two groups of 30 each using a computer-gene

Sponsors

Sanjay gandhi post graduate institute of medical sciences
Lead Sponsor
Dr Aneesh srivastava
Collaborator
Dr Gaurav sindwani
Collaborator
Dr Prabhaker mishra
Collaborator
Dr Sanjoy surekha
Collaborator
Dr Zakia saeed
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Renal transplant recepients between 18-65 years of age under general anaesthesia, Weight between 40-70kg

Exclusion criteria

Exclusion criteria: Refusal to participate in the study, Coagulopathy, Localized infection at the proposed site of injection, Psychiatric illness, Known allergy to local anaesthetics, Morbid obesity

Design outcomes

Primary

MeasureTime frame
To compare the total Fentanyl consumption in first 24 hour between Quadratus Lumborum versus placebo control group in renal transplant recepients. Timepoint: First 24 hour—

Secondary

MeasureTime frame
To compare the pain scores at rest between two groups using Numerical rating scale (0 to 10) in first 24 hrTimepoint: First 24 hr;To compare the pain scores on leg movements in between the two groups using Numerical rating scale (0 to 10) in first 24 hrTimepoint: First 24 hr;To compare the pain scores while coughing between the two groups using Numerical rating scale (0 to 10) in first 24 hrTimepoint: First 24 hr—

Countries

India

Contacts

Public ContactDr Sandeep sahu

Sanjay gandhi post graduate institute of medical sciences

drsandeepsahu@yahoo.co.in9235563953

Outcome results

None listed

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