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Not yet recruiting NCT06842160

Photoplethysmography (PPG) Algorithm with Smartwatch in Evaluation of Atrial Fibrillation Burden After Catheter Ablation

— Observational Atrial Fibrillation (AF)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: intervention group.
Who it may be relevant to
Registry conditions: Atrial Fibrillation (AF). Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose of this study is to evaluate the effectiveness of a smart electrocardiogram watch based on the PPG algorithm in monitoring the atrial fibrillation burden of patients after catheter ablation.

Interventions

  • Device intervention group
    A smart electrocardiogram watch based on the PPG algorithm for monitoring atrial fibrillation load after catheter ablation.

Primary outcome measures

  • Incidence of Stroke [Time frame: March 30, 2025 to March 30, 2035]
  • Incidence of Heart Failure [Time frame: March 30, 2025 to March 30, 2035]
  • All-Cause Mortality Rate [Time frame: March 30, 2025 to March 30, 2035]
  • Cardiovascular Mortality Rate [Time frame: March 30, 2025 to March 30, 2035]
  • Rate of Rehospitalization [Time frame: March 30, 2025 to March 30, 2035]
  • Incidence of Bleeding Events [Time frame: March 30, 2025 to March 30, 2035]
  • Postoperative Atrial Fibrillation Burden [Time frame: March 30, 2025 to March 30, 2035]

Eligibility criteria

Inclusion criteria

  • Atrial fibrillation patients diagnosed by electrocardiogram
  • Received catheter ablation procedure
  • Willing to use long-range electrocardiogram monitoring equipment

Exclusion criteria

1.Patients who are allergic to electronic devices or unable to wear watches

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Beijing Anzhen Hospital — Beijing

Identifiers

NCT: NCT06842160 · KS2024101 · KS2024101

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗