Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
NCT06421337

BraiN20® Medical Device in Suspected Acute Stroke Patients

Led by Alicia Martínez Piñeiro · Updated on 2024-05-20

500

Participants Needed

3

Research Sites

54 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Time is Brain company (http://www.tibtimeisbrain.com/about\_us/) developed BraiN20®, a medical device to assess the presence and characteristics of the N20 signal of SEP. Investigators have demonstrated a high prognostic accuracy of N20 on functional recovery of patients with acute ischemic stroke (AIS) due to large vessel occlusion (LVO) undergoing endovascular thrombectomy (EVT), the gold standard treatment. The aim if this new project is to validate BraiN20® in global patients presenting with suspected acute ischemic or hemorrhagic stroke in three comprehensive stroke centers in Spain. The primary objective is to establish the predictive performance of the presence of the N20 SEP over functional recovery as the primary outcome measure (likelihood of having a modified Rankin Scale (mRS) score 0-2 at 3 months evaluated by blinded independent raters). The effect will be measured by the metrics sensitivity, specificity, and predictive values, and compared with clinical and imaging predictive models by Receiving Operating Characteristics (ROC) curve analysis in the global population, stroke subtype and stroke mimics. Secondary aims are: 1) to determine the area under the curve (AUC) of the presence of the N20 SEP as biomarker of functional recovery in small subcortical infarctions and in patients with cortical infarctions and no large vessel occlusion; 2) to characterize N20 SEP signal in hemorrhagic stroke and stroke mimics; and 3) to evaluate the discriminant capacity of an explanatory new algorithm combining pre-hospital clinical variables and N20-SEP signal characteristics between ischemic, hemorrhagic and stroke mimics. This project would represent the first pilot study to validate the ability of BraiN20® to predict the functional recovery in the different types of acute stroke but also its ability to discriminate between stroke subtypes. Thus, BraiN20® monitoring could arise as a paradigm shift in acute stroke management, since it would standardize and accelerate patient triage, enable real time monitoring, increase access to EVT treatment and improve its outcome The trial is sponsored by Time is Brain S.L. and started in March 2024. Primary endpoint results are expected by the end of the 2024. BraiN20® could be a useful medical device aiding stroke subtype diagnosis and functional recovery.

CONDITIONS

Official Title

BraiN20® Medical Device in Suspected Acute Stroke Patients

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with suspected acute ischemic or hemorrhagic stroke admitted within 24 hours of symptom onset or last seen normal
  • Patients with stroke mimics confirmed after neurologic exam and diagnostics
  • Age 18 years or older
  • No significant functional dependence before stroke (mRS 0-2)
  • Baseline NIHSS score of 1 or higher (patients with TIA and full recovery excluded)
  • Ability to perform BraiN204 monitoring without delaying acute stroke treatments
  • Participation allowed if also enrolled in other treatment or diagnostic trials
  • Informed consent obtained from patient, surrogate, or deferred consent
Not Eligible

You will not qualify if you...

  • History of neuromuscular diseases or severe neurodegenerative disorders (mild cognitive impairment allowed), prior stroke (TIA allowed), or nervous system tumors interfering with SEP
  • Serious or terminal illness with life expectancy under 3 months
  • Women in premenopausal period
  • Presence of intracranial tumor (except small meningioma)
  • Use of demand-type cardiac pacemaker, defibrillator, or electrical implant or metal device
  • Suspected or known cancerous skin lesions where stimulation is applied
  • Localized wrist or forearm disorders (fractures, dislocations, vein puncture) where stimulation is applied

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Hospital Universitari de la Santa Creu i Sant Pau

Barcelona, Spain, 08025

Actively Recruiting

2

Hospital Universitari Arnau de Vilanova

Lleida, Spain, 25198

Actively Recruiting

3

Hospital Universitario La Princesa

Madrid, Spain, 28006

Actively Recruiting

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Research Team

A

Alicia Martinez, MD, PhD

CONTACT

A

Antoni Dávalos, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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