Atrial Fibrillation Trial, Recruiting NCT07058831 Sponsor: Cardiovascular Research Center Rosario British Sanatorium Condition: Atrial Fibrillation
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Atrial Fibrillation Trial, Recruiting

NCT07058831
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People of any sex who have high blood pressure and are older than 75 years of age
  • People with high blood pressure who are between 65 and 75 years old and also have at least one of the following conditions:
    • Obesity
    • Type 2 diabetes
    • Obstructive sleep apnea (breathing interruptions during sleep)
    • An ECG (heart tracing test) showing that the heart's left pumping chamber has become thickened or enlarged
    • An ultrasound of the heart showing that the left pumping chamber has become thickened or enlarged
    • An enlarged left upper chamber of the heart, detected by heart tests
    • Coronary artery disease (narrowing or blockage of the heart's main blood vessels)
    • Chronic kidney disease
    • A type of heart failure where the heart still pumps at a reasonable rate (confirm with trial site)
    • Regular alcohol intake
    • Frequent irregular heartbeats originating in the upper chambers of the heart

Who may not be able to join:

  • People who have ever had atrial fibrillation (a type of irregular heartbeat) of any kind
  • People currently taking medications that may affect heart rhythm
  • People with a history of serious, potentially dangerous irregular heartbeats originating in the lower chambers of the heart
  • People with an underactive or overactive thyroid that is not well controlled
  • People with significant chronic obstructive pulmonary disease (a serious long-term lung condition)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Daniel L Piskorz, MD, British Sanatorium Cardiovascular Research Center

Phone: 5493415416828

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Cardiovascular Research Center Rosario British Sanatorium
Registry
ClinicalTrials.gov
Start date
1 March 2025
Est. completion
30 December 2025

Where this trial is recruiting

🇦🇷 Argentina

Primary endpoints

new atrial fibrillation; The absolute numbers of patients with new atrial fibrillation; The percentage of patients with new atrial fibrillation

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov