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Lidocaine and Perioperative Cytokine Levels in Blood and Cerebrospinal Fluid in Cerebral Aneurysm Patients

Effect of Regional Anesthesia With Lidocaine on Perioperative Levels of Interleukin-1β, Interleukin-6 and Tumor Necrosis Factor-α in Blood and Cerebrospinal Fluid in Cerebral Aneurysm Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03823482
Enrollment
40
Registered
2019-01-30
Start date
2019-03-01
Completion date
2021-12-01
Last updated
2020-11-12

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

Conditions

Aneurysm, Cerebral

Keywords

aneurysm, cerebral, inflammation mediators, lidocaine, hydrochloride

Brief summary

Cerebral aneurysm surgery has significant mortality and morbidity rate. Inflammation plays a key role in the pathogenesis of intracranial aneurysms, their rupture, subarachnoid haemorrhage and neurologic complications. Brain injury activates immune cells and triggers cytokine release. Cytokine level in blood and cerebrospinal fluid is an indicator of inflammatory response. Cytokines contribute to secondary brain injury and can worsen the outcome of the treatment. Preventing secondary brain injury by modulating inflammatory response represents a therapeutic target. Lidocaine is local anesthetic that can be used in neurosurgery for regional anesthesia of the scalp and for topical anesthesia of the throat prior to direct laryngoscopy and endotracheal intubation. Except analgetic, lidocaine has systemic anti-inflammatory and neuroprotective effect. It acts through several mechanisms on various types of immune cells producing immunosuppressing effect. Lidocaine can act on activated microglia within central nervous system causing attenuation of immune response. Primary aim of this prospective randomized trial is to determine influence of lidocaine administration on inflammatory cytokine levels in serum and cerebrospinal fluid during and following cerebral aneurysm surgery. Secondary aim is to determine possible correlation between levels of cytokines and incidence of neurologic and infectious postoperative complications. For that purpose, postoperative neurological clinical status will be recorded. Signs of vasospasm and pathological postoperative brain CT scan findings will be recorded. Incidence of meningitis, pneumonia and sepsis in postoperative period will also be analyzed. Hypothesis of this trial is that lidocaine administration during cerebral aneurysm surgery would significantly change levels of pro-inflammatory cytokines in cerebrospinal fluid and serum. Lower concentrations of pro-inflammatory cytokines can possibly contribute to better outcome and significantly lower incidence of postoperative complications. Enzyme-immunochemical analysis will be used to measure levels of interleukin-1β, interleukin-6 and tumor necrosis factor-α in cerebrospinal fluid and serum. Investigation group will have, during cerebrovascular surgery under general anesthesia, regional anesthesia of the scalp and topical anesthesia of the throat prior to laryngoscopy, all done with lidocaine. Control group will have general anesthesia without lidocaine administration.

Interventions

DRUGLidocaine

Administration of lidocaine 2% 4 mg/kg administered as regional anesthesia of the scalp prior to Mayfield frame placement and lidocaine 1% 40 mg topically to the throat prior to direct laryngoscopy and endotracheal intubation.

Sponsors

Clinical Hospital Centre Zagreb
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* ASA ( American Society of Anesthesiologists) grading status I-III, * scheduled for cerebral aneurysm surgery under general anesthesia, * signed informed consent for participating in the research.

Exclusion criteria

* poorly controlled chronic or acute cardiovascular, respiratory or autoimmune disease, * acute infectious disease, * renal or hepatic insufficiency, * preoperative Glasgow Coma Scale score lower than 15, * allergic reaction to any of the medications in protocol, * pregnancy * refusal to participate in the research.

Design outcomes

Primary

MeasureTime frameDescription
Change in concentrations of tumor necrosis factor αUp to 24 hours after anesthesia induction.Concentrations of TNF-α in pg/ml in cerebrospinal fluid and serum measured by enzyme-linked immunosorbent assay
Change in concentrations of interleukin-1βUp to 24 hours after anesthesia induction.Concentrations of IL-1β in pg/ml in cerebrospinal fluid and serum measured by enzyme-linked immunosorbent assay
Change in concentrations of interleukin-6Up to 24 hours after anesthesia induction.Concentrations of IL-6 in pg/ml in cerebrospinal fluid and serum measured by enzyme-linked immunosorbent assay

Secondary

MeasureTime frameDescription
Incidence of vasospasmUp to one week postoperativelyFlow velocity over middle cerebral artery more than 180 cm/s measured by transcranial ultrasound
Incidence of pathological computerized tomography brain scanUp to one week postoperativelyFindings of edema, ischemia, bleeding or hydrocephalus on brain CT scan
Incidence of new motoric deficitUp to one week postoperativelyClinical assessment of neurologic status incidence of generalized epileptic seizure, incidence of vasospasm, pathological finding on brain computerized tomography ( ischemia, edema, bleeding, hydrocephalus).
Incidence of generalized epileptic seizureUp to one week postoperativelyClinical assessment to diagnose generalized epileptic seizure

Other

MeasureTime frameDescription
Incidence of meningitis, pneumonia and sepsisUp to one week postoperativelyClinical signs and laboratory findings for diagnosing infectious complications

Countries

Croatia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026