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Study of the QUadratus Lumborum Bloc in Total Hip ARthroplasty: Efficacy and Safety

Study of the QUadratus Lumborum Bloc in Total Hip ARthroplasty: Efficacy and Safety

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03189290
Acronym
SQUARE
Enrollment
100
Registered
2017-06-16
Start date
2017-07-06
Completion date
2018-09-10
Last updated
2019-04-22

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

Conditions

Postoperative Pain, Total Hip Replacement

Brief summary

The purpose of this prospective research study is to determine the best way to manage post-operative pain after a total hip arthroplasty. Currently, there is no standard of care for managing post-operative pain in these patients. The quadratus lumborum block (QLB) first described by Blanco in 2007, is a promising technique in this indication: recently, there is a growing evidence for the use of the QLB as an alternative technique for pain management after hip surgery.

Detailed description

A sample size of 100 patients (50 per group) was calculated based on 20% reduction in morphine consumption with 0.05% significance and a power of 0.8. After ethical committee approval, eligible patients scheduled to have a fast-track total hip arthroplasty are screened during preoperative evaluation clinic. Informed written consent will be obtained from all patients during pre-anesthesia visit the day before surgery (J-1). Consenting patients will be randomized the day of surgery (J0) to undergo QLB with ropivacaine (ropivacaine group) or normal saline (saline group). Before general anesthesia, all patients will have a needle-insertion posterior to the quadratus lumborum muscle avec injection of either ropivacaine in the ropivacaine group or normal saline in the saline group. After general anesthesia induction, dexamethasone and ketamine will be given to all patients.

Interventions

Procedure (experimental): ultrasound guided posterior Quadratus Lumborum Block (QLB) Procedure (experimental): Sham Block

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* American Society of Anesthesiologists Physical Classification Status (ASA) I to III * Age ≥ 18 years * Scheduled for fast-track total hip arthroplasty * Written informed consent * Patient covered by health insurance

Exclusion criteria

* Protected patients or patients incapable of giving written informed consent * Pregnant or breastfeeding woman * Vulnerable adult * Contraindication for fast-track surgery * Inability to comprehend or participate in pain scoring scales * Allergy to study drugs * Severe coagulopathy * Chronic kidney disease with glomerular filtration rate (GFR) ≤ 30 mL/min (estimated by the Cockcroft & Gault formula) * Chronic pain (treated by nonsteroidal anti-inflammatory drugs, opioids, neuroleptic drugs, antidepressant or anticonvulsants) * Peripheral neuropathy

Design outcomes

Primary

MeasureTime frame
Efficacy of the posterior quadratus lumborum block (QLB) versus placebo on morphine consumption during the first 24 hours after a total hip arthroplastythe first 24 hours after a total hip arthroplasty

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026