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
| Type | Name | Description |
|---|---|---|
| DEVICE | Implantation of ICRM | All 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.