Neutrophil Extracellular Traps and Thrombolysis in the Acute Stroke

Not Applicable

Completed

• Conditions: Acute Stroke
• Interventions: Procedure: Sample of Blood

• Registration Number: NCT02476188
• Lead Sponsor: Centre Hospitalier St Anne

Brief Summary

The purpose of the study was to investigate the correlation between the nucleosome concentration and the rate of recanalization after thrombolysis. All patients were admitted to the Stroke Unit at the University Hospital Sainte-Anne where they received standard stroke care. The investigators included all patients treated or not by intravenous thrombolysis for anterior circulation stroke with or without vessel occlusion. Exclusion criteria were neoplasms, chronic inflammatory diseases and cytostatic therapy at the time of stroke and stroke-specifics symptoms that had started earlier than 4.5 hours before admission.

Detailed Description

Neutrophil extracellular traps (NETs) were measured in serum at the time of hospitalization, then at 4 hours, 24 hours and 72 hours after stroke. Because of nucleosome instability, a strict preanalytical protocol was followed. Blood samples were centrifuged within 1-2 h after blood drawing. A strict preanalytical protocol was followed including early centrifugation of the samples and storage at - 80°C. NETs were quantified in batches containing all samples from a patient using the detection of MPO (myeloperoxidase) then the Cell-Death-Detection ELISAPLUS (Roche Diagnostics, Germany) as described earlier. Nucleosomes were quantified in relative arbitrary units (AU). Blood samples from each patient were measured within the same run to improve the comparability of the results.

For statistical analysis, various variables of nucleosomes were considered, such as the absolute concentrations determined at admission, at 24 hours and at 72 hours after stroke. Influence of nucleosome concentration on recanalization was tested. Continuous correlations of nucleosomes and infarction volume, nucleosomes and clot size, as well as of infarction volume and NIHSS were calculated by Spearman's rank correlation together with the 95% confidence interval. A p value \< 0.05 was considered statistically significant.

The extent of the morphological damage was determined at time of admission to the hospital and 24 hours after thrombolysis by diffusion-weighted magnetic resonance imaging (MRI). The pretreat¬ment and follow-up DWI lesions was segmented using interactive tools based on DWI signal intensity thresholding within a 3-dimensional mask encompassing the apparent area of bright DWI signal intensity and morphometric filtering. The clot location and length were assessed on the susceptibility vessel sign on T2\* as describe earlier.

Study Timeline

• Study First Submitted: 2015-06-11
• Study First Submitted QC: 2015-06-16
• Study First Posted: 2015-06-19
• Study Start: 2015-07-31
• Primary Completion: 2016-08
• Study Completion: 2016-11
• Status Verified: 2017-10
• Last Update Submitted: 2017-10-18
• Last Update Posted: 2017-10-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 124

Inclusion Criteria

• Patients ("Patients" + "Patients control" groups) :

Inclusion-1st sample of blood : every patient recruited within the neurovascular unit of intensive care of the Hospital center Sainte - Anne within the framework of a "thrombolyse alert ".

Then pursuit of the study ("patients" group only) if :

• Age 18 minimum
• Sylvien Infarct proved by the intellectual MRI,
• Whatever is the treatment received (Aspegic, thombolysis and/or thrombectomy)
• That there is occlusion of a cerebral artery or not "Controls" group :
• Healthy subjects,
• Mated on the age and the vascular risk factors (tobacco, arterial high blood pressure, diabetes and dyslipidémie)

Exclusion Criteria

• Patients:

• Contraindications in the intravenous thrombolysis according to the current recommendations .

  • Controls:

• Histories of evolutionary pathology or thrombo-embolique, taken by treatment whatever it is except contraceptive for the women, the viral or bacterial infection in the month precedents

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Patients	Sample of Blood	Samples of blood at H0, H+6, H+24 and H+72
Patients control	Sample of Blood	Samples of blood at H0
Control (healthy person)	Sample of Blood	Samples of blood at H0

Primary Outcome Measures

Name	Time	Method
Rate of recanalisation	24 hours	Correlation between NETs and stroke severity

Secondary Outcome Measures

Name	Time	Method
Thrombus size on MRI	24 hours	Correlation between NETs and stroke severity
Stroke volume on MRI	24 hours	Correlation between NETs and stroke severity

Trial Locations

Locations (1)

Centre Hospitalier Sainte-Anne; 🇫🇷 Paris, France