Actively Recruiting
Atrial Fibrillation in Active Cancer Patients
Led by University Hospital, Caen · Updated on 2024-08-09
1000
Participants Needed
1
Research Sites
226 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Caen
Lead Sponsor
U
University Hospital, Marseille, France
Collaborating Sponsor
AI-Summary
What this Trial Is About
Atrial fibrillation is a common complication of both cancer and anticancer drugs but the consequences of such events remain poorly known and are not adressed in both phase III oncological trials and cardiological guidelines. The objective of this study is to create a prospective multicenter international registry of adult patients with an active cancer and experiencing atrial fibrillation to study major cardiovascular events occurrence during a 1 year follow-up.
CONDITIONS
Official Title
Atrial Fibrillation in Active Cancer Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients
- Outpatients or hospitalized patients
- Confirmed cancer excluding basal-cell or squamous-cell carcinoma of the skin, primary brain tumor, known intracerebral metastases, or acute leukemia
- Active cancer defined as diagnosed within past 6 months or recurrent locally advanced or metastatic cancer
- Receiving anticancer treatment at enrollment or within 6 months before enrollment
- At least one episode of atrial fibrillation (new onset after cancer diagnosis or recurrence after cancer diagnosis)
- In sinus rhythm at time of cancer diagnosis
You will not qualify if you...
- Patients receiving palliative care or with conditions leading to expected death within one month after atrial fibrillation occurrence
- History of long-standing persistent or permanent atrial fibrillation prior to cancer diagnosis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Alexandre
Caen, Normandy, France, 14000
Actively Recruiting
Research Team
J
Joachim Alexandre, MD, PhD
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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