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NCT05762159
Analgesic Territory Assessment of the Spinal Erector Block Using Pupillometry
Conditions: Anesthesia, Local
Sex: All
Ages: 18 Years – N/A
Enrollment: 40
Sponsor: Centre Hospitalier Universitaire de Saint Etienne
Location: France
Summary
Few works have studied the area of analgesia covered by the spinal erector block in an objective manner, especially on the cephalo-caudal spread.
The available data are dissection works or subjective data such as thermoalgesic or epicritic sensitivity.This information would however be relevant in order to propose a better analgesia.
Indeed, it could explain certain failures by insufficient diffusion of the block.
The use of a multistage block could be relevant, especially in the case of osteosynthesis on several vertebral levels.
Eligibility Criteria
Inclusion Criteria:Patients receiving erector spinae block for pain management of spinal osteosynthesisExclusion Criteria:Patient refusalKnown allergy to local anestheticsContraindication to locoregional anesthesia (haemostasis disorder, infection, peripheral neuropathy)Technical impossibility to perform a spinal erector blockPathology with dysautonomia altering the pupillary reflex: diabetes mellitus with diabetic retinopathy, multiple sclerosis, systemic amyloidosis, uncontrolled hypertension, glaucomaCurrent treatment likely to alter pupillary dilation reflex to pain : antiemetic (droperidol, metoclopramide), alpha-2 agonist (clonidine)Serious psychiatric historyDrug abusePregnancy
Source: ClinicalTrials.gov (NCT05762159). StuddyBuddy aggregates publicly available trial information.