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NCT Number: NCT04776642

Biobank for "Arrhythmia and Conduction Disorders: TowArd Pathophysiology Based Treatment"

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Amsterdam University Medical Center location AMC

Amsterdam, Netherlands

Location status: Recruiting

About this study

The pathophysiological process of many cardiac arrhythmias is complex because of its multifactorial character. Despite extensive research that has already been performed in the field of electrophysiology the exact pathophysiological process of the different arrhythmias remains incompletely understood. The ability to identify subgroups of patients within a population with the same type of arrhythmia that can benefit from a specific treatment strategy might provide more individualized therapeutic opportunities, improve prognostication or provide preventive opportunities in patient with cardiac arrhythmias. Biobanks can make a valuable contribution to the development of diagnostic, preventive and therapeutic methods. More insights into the correlations between genes, environmental factors and susceptibility to illness may be of great value. The 'ADAPT' Biobank has been designed to establish a systematic and qualitative collection of bodily materials for future research in the cardiovascular field. The Biobank includes bodily material of patients with cardiac arrhythmias undergoing (non-) invasive treatment or control patients undergoing cardiothoracic surgery. Clinical data related to the cardiac arrhythmic disease is recorded. The data and samples will be linked to the participants' medical records to allow longitudinal follow-up.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients visiting the AMC outpatient clinic
  • Patients included in an ongoing clinical trial linked to this biobank. Studies are listed under point "Groups and interventions" and include:
  • MARK AF
  • INDICO AF
  • PREDICT AF
  • WEIGHTLOSS AF
  • MAD AF
  • Patients included in future clinical trial linked to this biobank. Studies may be linked to this biobank that investigates prevalent or incident cardiac arrhythmias.
  • Cardiac arrhtymias are defined as
  • Supraventricular tachycardia, among which the most common are:
  • Atrial Fibrillation (AF)
  • Atrial Tachycardia (AT)
  • Atrial Flutter (AFL)
  • Atrioventricular Nodal Reentrant Tachycardia (AVNRT)
  • Atrioventricular Reentrant Tachycardia (AVRT)
  • Ventricular tachycardia, among which the most common are:
  • Ventricular Tachycardia (VT)
  • Ventricular Flutter (VFL)
  • Ventricular Fibrillation (VF)
  • Bradycardia:
  • Sinus Node Dysfunction
  • AV Node Dysfunction
  • Interventricular Conduction Disorder
  • Arrhythmogenic cardiomyopathies, among which the most common are:
  • Dilated Cardiomyopathy
  • Restrictive Cardiomyopathy
  • Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Exclusion criteria

(shared for all studies):

  • Age < 18
  • Unable or unwilling to comply with study procedures
  • Pregnancy or of childbearing potential without adequate contraception
  • NYHA class IV heart failure symptoms or left ventricular ejection fraction <35%.

Treatment and study plan

Biobank for Left atrial appendage tissue

Other

Bodily material is used for biochemical marker assessments, histological and molecular analyses for research in cardiac arrhythmias.

Biobank for Blood

Other

Bodily material is used for biochemical marker assessments, histological and molecular analyses for research in cardiac arrhythmias.

Biobank for One or more of following fat patches: epicardial fat, subcutaneous fat, pericardial fat, visceral fat.

Other

Bodily material is used for biochemical marker assessments, histological and molecular analyses for research in cardiac arrhythmias.

Primary outcomes

  1. (new onset) atrial fibrilation

    Time frame: 5 year follow up

    obtain a comprehensive collection of patient information and material to facilitate research and gain better insight into the complex pathophysiology of the different arrhythmias

  2. recurrence of cardia arrythmia

    Time frame: 5 year follow up

    obtain a comprehensive collection of patient information and material to facilitate research and gain better insight into the complex pathophysiology of the different arrhythmias

Study contacts

Contact information is provided by the study sponsor or research team.

Elise Hulsman, Bc RN

CONTACT

[email protected]

31205665653

Joris de Groot, MD, PhD

CONTACT

[email protected]

310205666555

Sponsors and collaborators

Lead sponsor

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Other

Registry information

Official study title

"Arrhythmia and Conduction Disorders: TowArd Pathophysiology Based Treatment" ADAPT Biobank

Acronym: ADAPT

Important dates

Study start
2014
Primary completion
2030
Study completion
2030
First posted
Mar 2, 2021
Registry last updated
Jan 25, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.