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Clinical Trials/NCT03425162
NCT03425162CompletedNot Applicable

Ultrasound Guided Anterior Quadratus Lumborum Block for Postoperative Pain After Percutaneous Nephrolithotomy: Randomized Controlled Trial

Bursa Yüksek İhtisas Education and Research Hospital1 site in 1 country60 target enrollmentStarted: February 12, 2018Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Visual Analog Scale

Study Overview

Brief Summary

Percutaneous nephrolithotomy (PNL) is frequently used today for renal stones. percutaneous nephrolithotomy (PNL) procedure has become the treatment of choice for many patients with symptomatic renal stones . Patients undergoing PNL suffer from acute postoperative pain, despite a multimodal analgesic regime.

This is a randomised controlled trial efficacy of the anterior Quadratus Lumborum Block (QLB) in terms of analgesic efficacy in patients who undergo percutaneous nephrolithotomy.

Detailed Description

Many analgesic procedures such as NSAID, opioid and regional anesthesia procedures are used as a part of multimodal analgesia for postoperative Percutaneous nephrolithotomy pain.

In this study we will use the ultrasound -guided anterior Quadratus Lumborum Block . Local anesthesic will be injected between quadratus lumborum muscle and psoas muscle with ultrasound.Analgesic effect of this block will be detected by using morphine consumption and visual analogue scale .

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients who were in the American Society of Anesthesiologists (ASA) I-III class and underwent elective Percutaneous nephrolithotomy

Exclusion Criteria

  • Previous history of opioid use preoperatively,
  • Allergy to local anesthetics,
  • The presence of any systemic infection,

Arms & Interventions

Group A

Active Comparator

Group A:Ultrasound guided unilateral anterior Quadratus Lumborum block with 20 ml %0.25 bupivacaine+PCA (morphine)

Intervention: Morphine Sulfate (Drug)

Group A

Active Comparator

Group A:Ultrasound guided unilateral anterior Quadratus Lumborum block with 20 ml %0.25 bupivacaine+PCA (morphine)

Intervention: Group A (Procedure)

Group P

Sham Comparator

Group P:PCA (morphine)

Intervention: Morphine Sulfate (Drug)

Group P

Sham Comparator

Group P:PCA (morphine)

Intervention: Group P (Procedure)

Outcomes

Primary Outcomes

Visual Analog Scale

Time Frame: Postoperative 24 hours

Visual Analog Scale was used for pain.Pain intensity was measured using 0-10 cm visual analogue scale (VAS). (0= no pain, 10=intolerable pain)

Secondary Outcomes

  • morphine consumption(Postoperative 24 hours)
  • additional analgesic use(Postoperative 24 hours)
  • side effect profile(Postoperative 24 hours)

Investigators

Sponsor
Bursa Yüksek İhtisas Education and Research Hospital
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Korgün Ökmen

Principal Investigator

Bursa Yüksek İhtisas Education and Research Hospital

Study Sites (1)

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