NCT03611816

Brief Summary

Atrial fibrillation (AF) is the most common cardiac arrhythmia encountered in clinical practice. This arrhythmia is responsible for 15% of strokes and more than 30% of strokes on people over 65 years. According to studies, 30 to 40% of isolated atrial fibrillations could be familial. Atrial fibrillation has significant genetic heterogeneity. About 40 genes have been identified as potentially involved. Studies have identified genes common to the risk of atrial fibrillation and stroke. Despite the pathophysiology of atrial fibrillation has been intensively and extensively studied for almost a century, there are still many questions. The pathophysiology is not sufficiently understood to allow finding more effective therapies. It is necessary to identify genetic determinants and thus potentially new pharmacological targets more adapted. The establishment of a biological database will test hypotheses concerning the genetic origin and thromboembolic process of atrial fibrillation and associated stroke.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
85mo left

Started Apr 2018

Longer than P75 for all trials

Geographic Reach
1 country

5 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress54%
Apr 2018Apr 2033

First Submitted

Initial submission to the registry

January 31, 2018

Completed
3 months until next milestone

Study Start

First participant enrolled

April 23, 2018

Completed
3 months until next milestone

First Posted

Study publicly available on registry

August 2, 2018

Completed
14.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 23, 2033

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 23, 2033

Last Updated

April 17, 2026

Status Verified

April 1, 2026

Enrollment Period

15 years

First QC Date

January 31, 2018

Last Update Submit

April 16, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Quality of DNA sample

    Quality is based on the measure of the purity of DNA with absorbance assay at 260/280nm on a spectrophotometer. For Plasma sample, purity is based on absence of hemolyzed blood by visual observation.

    1 day (the day of the storage)

  • Quality of Plasma sample

    Quality is based on the purity of Plasma sample that is based on absence of hemolyzed blood by visual observation.

    1 day (the day of the storage)

  • Quality of preservation of the sample

    The quality of preservation of the sample throughout the conservation duration is based on the number of freezing/thawing of each cryotube that will be notified. As weel as any interruption in the freezing process (power failure, freezer failure).

    7 years (during all the duration of the collection)

Study Arms (5)

Group 1a

Patient with atrial fibrillation and without stroke history.

Biological: Blood takenGenetic: Blood taken

Group 1b

Patient with atrial fibrillation with scheduled electrophysiology exploration or ablation.

Biological: Blood takenGenetic: Blood taken

Group 1c

Patient with atrial fibrillation and with stroke history.

Biological: Blood takenGenetic: Blood taken

Group 2

Patients aged over 80 years old and without history of atrial fibrillation.

Biological: Blood takenGenetic: Blood taken

Group 3

Patient with cryptogenic stroke or transient ischemic attack history before the age of 50.

Biological: Blood takenGenetic: Blood taken

Interventions

Blood takenBIOLOGICAL

Collection of clinical data

Group 1aGroup 1bGroup 1cGroup 2Group 3

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Atrial fibrillation patient Stroke patient Patient over 80

You may qualify if:

  • \- AF history

You may not qualify if:

  • No AF history
  • patient who didn't signed consent
  • Group 1b
  • AF history
  • Scheduled electrophysiological exploration or AF ablation
  • No AF history
  • pregnant women
  • patient who didn't signed consent
  • Group 1c
  • AF/AT history
  • Stroke history
  • No Stroke history
  • patient who didn't signed consent
  • Group 2
  • patient over 80
  • +14 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (5)

Service neurologie Centre hospitalier Fleyriat

Bourg-en-Bresse, 01000, France

RECRUITING

Service d'urgences Neurovasculaires - service de neurologie vasculaire , Hôpital Pierre Wertheimer

Bron, 69677, France

RECRUITING

Service de rythmologie, hôpital cardiologique Louis Pradel

Bron, 69677, France

RECRUITING

Service de médecine gériatrique Centre hospitalier Lyon Sud, Groupement hospitalier Sud

Pierre-Bénite, 69495, France

RECRUITING

Hôpital des charpennes

Villeurbanne, 69100, France

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

DNA, plasma

MeSH Terms

Conditions

StrokeAtrial Fibrillation

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesArrhythmias, CardiacHeart DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 31, 2018

First Posted

August 2, 2018

Study Start

April 23, 2018

Primary Completion (Estimated)

April 23, 2033

Study Completion (Estimated)

April 23, 2033

Last Updated

April 17, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations