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Clinical Trials in France / NCT04670224
Active, not recruiting Not applicable

Efficiency of the Quadratus Lumborum Block for Post-operative Analgesia in Abdominoplasty Surgery

NCT04670224 · tracked via the Priya Life Science France tracker
Sponsor
Centre Hospitalier Universitaire, Amiens
Phase
Not applicable
Started
2021-03-16
Last updated
2025-05-29

Condition(s) studied

Quadratus Lumborum BlockAbdominoplastyAnalgesiaLocoregional Anesthesia

Investigational drug(s) / intervention(s)

QLB anesthesiaIntravenous anesthesia without QLB

QLB anesthesia: The QLB is a bilateral locoregional anesthesia technique, performed after surgery, under general anesthesia and in right and then left lateral decubitus.

Intravenous anesthesia without QLB: only intravenous anesthesia

Study summary

Abdominoplasty is a common surgical procedure in plastic surgery which causes postoperative pain and may delay patients' recovery. Surgery is potentially associated with a number of postoperative complications, whether cardiovascular, respiratory, infectious, thromboembolic, or digestive … Although they do not inevitably lead to a life-threatening prognosis, in many cases these complications delay post-operative recovery. Defined in the 1990s by Professor Henry Kehlet's Danish team, rapid rehabilitation after planned surgery is an approach to overall patient care that aims to rapidly restore previous physical and mental capacities and thus significantly reduce mortality and morbidity. Pain management is at the heart of this program and local anesthesia techniques are at the heart of early rehabilitation programs.

Described for just over a decade, Quadratus Lumborum Block (QLB) have shown their effectiveness for analgesia in abdominal, or orthopedic, or obstetrical surgery. Considering the anatomical territory concerned, this locoregional anesthesia technique seems to be very interesting in abdominoplasty to allow early rehabilitation of the patient.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patients admitted for programmed dermo-lipectomy surgery with or without associated liposuction. Exclusion Criteria: * Pregnant woman * Patient under 18 years of age * Subject under guardianship or curators * Patient allergic to local anesthetics * Infection at the puncture sites * Patient on morphine analgesic over the long term * Patient on antidepressants for neuropathic pain.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
BAR Amiens France

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Other trials for the same condition

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Sufentanil Versus Ketamine Intranasally in the Management of Severe Acute Trauma-related Pain in Children. Starting soon
Postoperative Analgesia Using a Perineural Catheter Versus a Single Nerve Block in Rearfoot Surgery Recruiting
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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04670224 on ClinicalTrials.gov ↗ ← All trials in France