Systematic Assessment of Treatment Effectiveness for Long-Term Management of Stable Atrial Tachycardia in Inpatient and Outpatient Environments

The aim is to analyze long-term outcomes in a multicenter observational registry including patients undergoing atrial tachycardia rhythm control.

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Key information

Conditions

Atrial Tachycardia Arrhythmias, Cardiac Atrial Flutter Brain Diseases Cardiovascular Diseases Central Nervous System Diseases Cerebrovascular Disorders Heart Diseases Mortality Nervous System Diseases Pathologic Processes Pathological Conditions, Signs and Symptoms Stroke Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

EVK Düsseldorf, Düsseldorf, Germany

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Patients undergoing atrial tachycardia rhythm control

Exclusion criteria

Follow-up <30 days after atrial tachycardia rhythm control

Treatment and study plan

Primary outcomes

Mortality, stroke and cardiovascular hospitalization

Time frame: From AT rhythm control through study completion, an average of 2 years

Sponsors and collaborators

Lead sponsor

Evangelical Hospital Düsseldorf

Other

Collaborators

Asklepios Klinik St. Georg
Münster University Hospital, Germany
Staedtisches Klinikum Karlsruhe
Universitätsklinikum Hamburg-Eppendorf

Registry information

Acronym: SATELLITE

Important dates

Study start: 2024
Primary completion: 2026
Study completion: 2026
First posted: Nov 20, 2025
Registry last updated: Nov 20, 2025

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.

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