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D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation of Atrial Fibrillation

G

Groupe Hospitalier de la Rochelle Ré Aunis

Status

Completed

Conditions

Atrial Fibrillation

Treatments

Other: D-dimer assay before ablation of atrial fibrillation

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02199080
2014/P02/001
2013-A01700-45 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to determine whether D-dimer dosage allow to exclude risk of intraatrial thrombus before performing an ablation of atrial fibrillation

Enrollment

2,506 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age> 18 years.
  • Patients hospitalized for ablation of atrial fibrillation or symptomatic left flutter
  • Patient informed of the study

Exclusion criteria

  • Age <18 years.
  • Patients under guardianship
  • Pregnant woman
  • Contraindication to transesophageal echocardiography
  • transesophageal echocardiography made in another center as the center of ablation
  • Refusal of the patient to participate in the study
  • Patient participating in another interventional study in which an intervention related to biomedical research is performed before the transesophageal echocardiography

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

2,506 participants in 1 patient group

Atrial fibrillation
Other group
Description:
D-dimer assay before ablation of atrial fibrillation
Treatment:
Other: D-dimer assay before ablation of atrial fibrillation

Trial contacts and locations

37

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Data sourced from clinicaltrials.gov

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