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Erector Spinae Plane Block After Lumbar Spinal Stenosis Surgery

Impact of the Erector Spinae Plane Block on the Postoperative Pain After Lumbar Spinal Stenosis Surgery: Single Blind Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04403360
Enrollment
80
Registered
2020-05-27
Start date
2018-10-01
Completion date
2021-04-01
Last updated
2020-05-27

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

Conditions

Lumbar Spinal Stenosis, Erector Spinae Plane Block

Brief summary

Lumbar spinae stenosis surgery is a frequent intervention resulting in important postoperative pain. Management of this postoperative pain is thus important. Different pain management therapies exist. The erector spinae plane (ESP) block was described in 2016. It involves the injection of local anesthetics into the interfascial plane, deep to erector spinae muscle, allowing the blockade of the dorsal and ventral rami of the thoracic spinal nerves. It was initially proposed for analgesia of costal fractures, pulmonary lobectomy and thoracic vertebrae. The ESP block (ESPB) could probably be extended to a large number of surgical procedures. ESPB has so far not been investigated in lumbar spinae stenosis surgery.

Interventions

PROCEDUREESPB

Ultrasound guided performance of ESPB at T12 level after the induction of anesthesia but before the start of the surgery

PROCEDURELocal infiltration by the surgeon

Local infiltration of anesthetics at surgical site after skin incision

Sponsors

Clinique Saint Pierre Ottignies
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

\- Any lumbar spinae surgery on 2 or more lumbar levels

Exclusion criteria

* Contraindication to NSAID * Allergy to any local anesthetics

Design outcomes

Primary

MeasureTime frameDescription
Total 24 h Piritramide consumption24 hoursTotal consumption of Piritramide consumption after surgery

Secondary

MeasureTime frameDescription
Quebec back pain disability scale (QBPDS)At 2 months]A questionnaire developed to measure the level of functional disability for patients with low back pain

Countries

Belgium

Contacts

Primary ContactGeorges SAMOURI, MD
georges.samouri@cspo.be003210437260
Backup ContactNicolas PARISI, MD
nicolas.parisi@cspo.be003210437608

Outcome results

None listed

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