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N/A N=30 Treatment

Vesalio NeVa VS for Symptomatic Cerebral Vasospasm Following aSAH (The VITAL Study)

Cerebral Vasospasm

Enrolled (actual)
30
Serious AEs
56.7%
Results posted
Jan 2023
Primary outcome: Primary: Procedural Success — 64 Vessels Treated

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
NeVa VS (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Vesalio
Primary completion
May 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Procedural Success
64

Summary

The objective of the study is to assess the safety and probable benefit of the Neva VS device in patients presenting with symptomatic cerebral vasospasm despite maximal medical management following aSAH.

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years.
  • Subarachnoid hemorrhage secondary to ruptured aneurysm.
  • Ruptured aneurysm secured with surgical clipping or endovascular intervention.
  • Digital subtraction angiography (DSA) or CT angiography at the time of aSAH clinical presentation or aSAH intervention with well-visualized intra-cerebral vessels is available for review.
  • Vasospasm in one or more of the following: the internal carotid artery (ICA), basilar, middle cerebral artery (MCA), anterior cerebral artery (ACA), or posterior cerebral artery (PCA) territory on transcranial Doppler (TCD), and/or CT angiography, and/or clinical signs of symptomatic vasospasm (change in level of consciousness, focal neurological deficit) confirmed by > 50% narrowing in these territories on DSA.
  • Vasospasm despite maximized medical management defined as oral Nimodipine (unless contraindicated), systemic hypertension with SBP greater than 130 mmHg and euvolemia.
  • Target vessel pre-vasospasm diameter ≥ 2 mm and ≤ 4.0 mm.
  • Subject or legal representative is able and willing to give informed consent.

Exclusion Criteria

  • The presence of an unsecured ruptured aneurysm. Note unsecured unruptured aneurysms remote to the site of treated aSAH are not an exclusionary.
  • Symptoms attributable to other causes (e.g., hydrocephalus, metabolic, infection).
  • Hunt and Hess Grade of 5
  • Large infarct on CT scan defined as ASPECTS 0-5.
  • Intracranial hemorrhage not caused by aneurysm rupture.
  • History of bleeding disorders.
  • Baseline platelets 1.7.
  • Any known contraindications to mechanical dilation of vasospastic vessels including but not limited to:
  • Excessive vessel tortuosity that prevents the placement of the device
  • Evidence of rapidly improving neurological signs of stroke
  • Large territory completed cerebral infarction, edema with mass effect and intra-parenchymal hemorrhage in vascular territory to be treated, or
  • any other vascular anatomic variants or anomalies
  • Pre-existing neurological or psychiatric disease that would confound the neurological or functional evaluations, e.g. dementia with prescribed anti-cholinesterase inhibitor (e.g. Aricept).
  • History of severe allergy to contrast medium.
  • Known allergy to NeVa materials (nitinol, stainless steel).
  • Suspected or confirmed septic embolus, or bacterial endocarditis.
  • Septic shock or central nervous system (CNS) infection confirmed via cerebrospinal fluid (CSF) sampling.
  • Known current or recent use of illicit drugs or alcohol abuse.
  • Females who are pregnant or breastfeeding.
  • Any other condition that, in the opinion of the investigator, precludes an endovascular procedure or poses a significant hazard to the subject if an endovascular procedure is performed.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03611790). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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