Actively Recruiting
MANAGE-AF Registry -MANAGEment of Atrial Fibrillation Outcomes Registry (MANAGE-AF)
Led by CorVita Science Foundation · Updated on 2024-01-18
1000
Participants Needed
1
Research Sites
523 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this research is to learn more about the normal care of patients with a new or pre-existing diagnosis of atrial fibrillation (AF). These abnormal and irregular heartbeats place patients at increased risk of developing clots in their bloodstream that could potentially lead to stroke. Normal care is designed to help prevent this from happening and to lessen or eliminate the symptoms patients may have. There are many different types of AF as well as numerous ways in which a variety of patients are treated. The investigators are interested in gathering more information to better keep track of patient treatment patterns (trends) that may differ from physician to physician, hospital to hospital, medication to medication, patient to patient and if necessary, procedure to procedure.
CONDITIONS
Official Title
MANAGE-AF Registry -MANAGEment of Atrial Fibrillation Outcomes Registry (MANAGE-AF)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of valvular or non-valvular atrial fibrillation
- ECG documented atrial fibrillation by 12 lead, rhythm strip, event monitor, Holter monitor, or implantable loop recorder
- Age 18 years or older
You will not qualify if you...
- Younger than 18 years
- Clinical evidence that death within 6 months is possible
- Unable to consent to the research or sign a consent form
- Unable to follow up at the research clinic at least annually for continuity of AF care and management
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CorVita Science Foundation (NFP)
Chicago, Illinois, United States, 60605
Actively Recruiting
Research Team
E
Edward M Burke
CONTACT
M
Martin C Burke, DO
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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