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Correlation Between Laboratory Markers and Origin of New Brain Ischemic Lesions After Carotid Stenting

U

University Hospital Ostrava

Status

Completed

Conditions

Brain Ischemia
Carotid Stenosis
Laboratory Problem

Treatments

Procedure: Carotid stenting

Study type

Observational

Funder types

Other

Identifiers

NCT02310191
UHOG-2/2012

Details and patient eligibility

About

New brain ischemic lesions are detected in about 50% of patients undergoing carotid artery stenting (CAS). The aim was to assess correlation between selected laboratory markers and occurrence of new brain infarctions after CAS.

Full description

Methods: All consecutive patients 1) with internal carotid artery stenosis >70%, 2) indicated to CAS, 3) with signed informed consent were enrolled to the prospective study during 16 months. All patients used dual antiplatelet therapy (acetylsalicylic acid [ASA] 100 mg + clopidogrel 75 mg per day) at least 7 days before CAS. Neurological examination and brain magnetic resonance imaging (MRI) were performed before and 24 hours after CAS in all patients. Venous blood samples were collected within 24 hours before CAS in all patients: hematology + reticulocytes, coagulation markers (PT, APTT, INR, Fbg, Clauss), vWF antigen, PAI-1 activity, PAI-1 polymorphism 4G/g, Multiplate (ASA and clopidogrel resistance test). Blood samples for the assessment of anti Xa activity were collected during CAS. T-test was used for statistical evaluation.

Enrollment

81 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

patients

  1. With internal carotid artery stenosis >70%
  2. Indicated to CAS
  3. With signed informed consent. Able to use (acetylsalicylic acid [ASA] 100 mg + clopidogrel 75 mg per day) at least 7 days before CAS

Exclusion criteria

  • Contraindication for magnetic resonance imaging

Trial design

81 participants in 1 patient group

Stenting
Description:
Carotid stenting
Treatment:
Procedure: Carotid stenting

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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