ClinicalTrials.Veeva

Menu

Blood Biomarkers to Predict the Prognosis of a Stroke Patient Undergoing Mechanical Thrombectomy (TROMBOPOCT)

F

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

Status

Enrolling

Conditions

Acute Ischemic Stroke

Treatments

Device: Large Vessel Occlusion Biomarkers Test

Study type

Observational

Funder types

Other

Identifiers

NCT06467396
TROMBOPOCT

Details and patient eligibility

About

The goal of this observational study is to evaluate the accuracy of a panel of blood biomarkers and clinical variables in predicting the prognosis of stroke patients treated by mechanical thrombectomy, specifically to predict futile recanalization and mortality.

Full description

Stroke is the leading cause of long-term disability and the second most common cause of death worldwide, accounting for around 6.7 million deaths each year. The burden of stroke due to illness, disability and early death is set to double within the next 15 years due to an ageing population. The socio-economical cost of the stroke is very high, being around 45 million euros per year in Europe. Although mechanical thrombectomy is the most effective treatment for stroke patients with large vessel occlusions still a large percentage of patients, around 50%, do not recover despite a successful recanalization (the so called "futile recanalization"). Therefore, to anticipate the prognosis of patients treated with mechanical thrombectomy would be clinically relevant and very informative.

This observational study evaluates the precision of a rapid test of blood biomarkers in the prognosis of stroke patients treated by mechanical thrombectomy. For that, the investigators will recruit a cohort of 400 consecutive patients treated by thrombectomy. Using a multiplex POC for the biomarker measurement and an APP in combination with clinical data, the potential of biomarkers to predict the prognosis of a patient will be determined.

Enrollment

400 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients > 18 years old.
  • Patient in whom a mechanical thrombectomy is performed.

Exclusion criteria

  • Impossibility of getting a blood sample.
  • Impossibility of performing the test (Invalid results)
  • Refusal to provide the informed consent by the patient/relative.

Trial contacts and locations

2

Loading...

Central trial contact

Rosa M Delgado; Carmen De Jesús Gil

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems