Clinical Trials Directory

Trials / Completed

CompletedNCT02725944

Prediction and Detection of Occult Atrial Fibrillation in Patients After Acute Cryptogenic Stroke and TIA

Prediction and Detection of Occult Atrial Fibrillation in Patients After Acute Cryptogenic Stroke and Transient Ischemic Attack

Status
Completed
Phase
Study type
Observational
Enrollment
251 (actual)
Sponsor
University Hospital, Akershus · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

PROACTIA is a prospective, event-driven observational study. It aims to propose a composite scoring system in order to evaluate the risk of paroxysmal atrial fibrillation (PAF) in patients after acute cryptogenic stroke and transient ischemic attack (TIA).

Detailed description

It will be enrolled 250 participants of both sexes within two weeks after diagnosed cryptogenic stroke and/or TIA at Akershus University Hospital, Oslo area, Norway. Evaluation of participants' comorbidity with CHADS2-VASc score, ECG, Holter ECG, echocardiography, detection of biochemical cardiac markers and screening for obstructive sleep apnea syndrome will be performed. All participants will be monitored with a continuous cardiac rhythm during one year by implantation of implantable cardiac rhythm monitors (ICRM). All patients without high bleeding risk will get prescribed oral anticoagulants (OAC) after detection of PAF. A biobank will be established in order to store the sampled biological material.

Conditions

Interventions

TypeNameDescription
DEVICEImplantation of ICRMAll patients will be implanted with ICRM in order to detect an occult PAF.

Timeline

Start date
2016-05-15
Primary completion
2018-06-18
Completion
2018-06-18
First posted
2016-04-01
Last updated
2018-09-10

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT02725944. Inclusion in this directory is not an endorsement.