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Trials / Recruiting

RecruitingNCT06174506

The Role of hs Troponin I and NT-proBNP in Predicting Atrial Fibrillation in Patients With Permanent Pacemakers

Status
Recruiting
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
University of Medicine and Pharmacy at Ho Chi Minh City · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to answer the research question whether hs Troponin I and NT-proBNP have a role in detecting atrial fibrillation in patients with pacemakers. Objectives of the study: 1. To survey some risk factors for atrial fibrillation in patients with permanent pacemakers. 2. To determine the role of hs Troponin I and NT-proBNP in predicting new-onset atrial fibrillation within follow-up time. 3. To build a model to predict the prognosis of atrial fibrillation based on the detected subclinical markers related to atrial fibrillation and classic cardiovascular risk factors.

Detailed description

Information about age, gender, BMI, medical history, tests to evaluate liver function, kidney function, dyslipidemia, results of echocardiography, ECG, and chest X-ray will be collected from medical records and clinical examination. The hs troponin I and NT-proBNP tests will be performed before the patient has a pacemaker. The two tests above will be paid by research team. Patients do not have to pay for these tests. Atrial fibrillation will be determined through ECG, holter ECG and pacemaker data. Time to follow up patients in the study: According to the patient's follow-up visits after pacemaker placement: 1 month, 3 months, 6 months, then every 6 months.

Conditions

Timeline

Start date
2023-12-01
Primary completion
2026-09-30
Completion
2026-09-30
First posted
2023-12-18
Last updated
2023-12-18

Locations

1 site across 1 country: Vietnam

Source: ClinicalTrials.gov record NCT06174506. Inclusion in this directory is not an endorsement.