Actively Recruiting
Biobank for "Arrhythmia and Conduction Disorders: TowArd Pathophysiology Based Treatment"
Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2024-01-25
1000
Participants Needed
1
Research Sites
784 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The 'ADAPT' Biobank is a collection of body material and data from patients with or at risk of cardiac arrhythmias who underwent or will undergo (non-) invasive treatment for this disease. Its main objective is to obtain a comprehensive collection of patient information and material to facilitate research and gain better insight into the complex pathophysiology of the different arrhythmias, the multifactorial process, the heterogeneity in clinical presentation, and prognosis. Bodily material is used for biochemical marker assessments, histological and molecular analyses for research in cardiac arrhythmias.
CONDITIONS
Official Title
Biobank for "Arrhythmia and Conduction Disorders: TowArd Pathophysiology Based Treatment"
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients visiting the AMC outpatient clinic
- Patients included in an ongoing clinical trial linked to this biobank (such as MARK AF, INDICO AF, PREDICT AF, WEIGHTLOSS AF, MAD AF)
- Patients included in future clinical trials linked to this biobank investigating cardiac arrhythmias
- Patients with cardiac arrhythmias including supraventricular tachycardia (atrial fibrillation, atrial tachycardia, atrial flutter, AVNRT, AVRT), ventricular tachycardia (ventricular tachycardia, ventricular flutter, ventricular fibrillation), bradycardia (sinus node dysfunction, AV node dysfunction, interventricular conduction disorder), or arrhythmogenic cardiomyopathies (dilated, restrictive, ARVC)
You will not qualify if you...
- Age under 18 years
- Unable or unwilling to comply with study procedures
- Pregnancy or childbearing potential without adequate contraception
- NYHA class IV heart failure symptoms or left ventricular ejection fraction less than 35%
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Amsterdam University Medical Center location AMC
Amsterdam, Netherlands
Actively Recruiting
Research Team
E
Elise Hulsman, Bc RN
CONTACT
J
Joris de Groot, 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
7
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