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Microparticles Circulating Plasma Concentration in Atrial Fibrillation After Percutaneous Occluding of the Left Atrium (MICROPLUG)

I

Institut Mutualiste Montsouris

Status

Unknown

Conditions

Atrial Fibrillation

Treatments

Other: blood sampling

Study type

Observational

Funder types

Other

Identifiers

NCT03361202
CARDIO-01-2015

Details and patient eligibility

About

The aim of the study is to compare levels of differnts types of microparticles circulating before and after percutaneous occluding of the left atrium by patients with atrial fibrillation and patients control.

Hypothesis is that prothesis implantation will decrease levels of microparticles circulating in blood circulation because of occluding of the left atrium .

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

atrial fibrillation group:

  • high embolic risk (CHADS-VASC2 score ≥4)
  • formal and final contraindication to anticoagulant therapy
  • no heart thrombus on ETO and TDM before percuraneous occluding

control group:

  • suspicion of stable coronary artery disease, coronary angiography scheduled and double platelet aggregation (clopidogrel and aspirine)

Exclusion Criteria: for both groups

  • congestive heart failure, severe aortic stenosis, EP or TVP early.

Trial design

50 participants in 2 patient groups

Atrial fibrillation group
Description:
blood sampling
Treatment:
Other: blood sampling
control group
Description:
blood sampling
Treatment:
Other: blood sampling

Trial contacts and locations

1

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Central trial contact

Isabelle SAURET; Nicolas AMABILE, doctor

Data sourced from clinicaltrials.gov

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