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Comparison of Mean Duration of Post Operative Analgesia Following QL-2 Block vs QL-3 Block Using Ropivacain 0.25% in Patients Undergoing Unilateral Inguinal Hernia Repair

Q

Quaid-e-Azam Medical College

Status

Completed

Conditions

Inguinal Hernia Unilateral

Treatments

Procedure: Quadratus Lumborum (QL) Block

Study type

Interventional

Funder types

Other

Identifiers

NCT07200076
BVH-2025-CT-010

Details and patient eligibility

About

To compare the mean dulation of post operative analgesia following QL2 block (posterior quadratus lumborum block) and the QL3 block (transmuscular quadratus lumborum block) using ropivacaine 0.25% in patients undergoing unilateral inguinai hernia repair.

Rationale of the proposed study is to find an optimal approach for quadratus lumborum block (QLB) in the context of local population as no local study has already been carried out for our population. The study seeks to determine which approach provides superior postoperative pain relief and aspires to establish a clear rationale for the application of one technique over the other in local population. By uncovering the strengths and limitations of each approach, the study intends to guide local clinicians in making informed decisions for optimizing postoperative pain management strategies. The outcomes of this study are anticipated to have a substantial impact on clinical practice, potentially leading to improved patient outcomes, reduced opioid consumption, and enhanced patient comfort following inguinal hernia repair surgeries in local settings.

Enrollment

64 patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 18 and 50 years ASA status 1 or 2 Scheduled for unilateral inguinal hernia repair under General Anaesthesia

Exclusion criteria

  • Patient refusal Patients with pre-existing coagulation abnormalities INR more thnn 1.5 Patients with Strangulated hernia Hypersensitivity to local anaestiretics. Local infection at procedure sito.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

64 participants in 2 patient groups

QLB-2 (posterior QL block) Group
Active Comparator group
Treatment:
Procedure: Quadratus Lumborum (QL) Block
QLB-3 (transmuscular QL block) Group
Active Comparator group
Treatment:
Procedure: Quadratus Lumborum (QL) Block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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