Heart Disease Trial, Recruiting NCT06620653 Sponsor: National University of Ireland, Galway, Ireland Condition: Heart Disease
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Heart Disease Trial, Recruiting

NCT06620653
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:

  • Adults aged 18 or older who have recently been in hospital.
  • People who have had their heart pumping strength (ejection fraction) measured and whose heart failure stage (NYHA Class) is known.
  • People with either a previously diagnosed or newly identified heart failure condition.
  • People, or their carer, who can speak and understand English or Irish.
  • People who are willing to take part in the study.
  • People who live within the area served by the Saolta hospital group in Ireland.

Who may not be able to join:

  • People who do not wish to take part in the study.
  • People receiving palliative care or who have a life expectancy of less than one year.
  • People being discharged from hospital to a skilled nursing facility or nursing home.
  • People who have a planned procedure on the mitral or aortic heart valve during their hospital stay or shortly after discharge.
  • People who are planned to start kidney dialysis (haemodialysis).
  • People who are already taking part in another clinical trial.
  • People who, in the opinion of the study doctor, may not be able to fully participate — for example due to a history of not taking medications or attending follow-up appointments, a language barrier, or significant memory or thinking difficulties without the support of a family member or carer.
  • People whose heart is not pumping as strongly as it should, but who have no symptoms from it (NYHA Class I), particularly when this is related to a recent heart attack.
  • Note: Not being confident with technology does not prevent someone from being considered for this trial.

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 22 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: Derek O'Keeffe, MD, PhD, Galway University Hospitals/University of Galway

Phone: +353 861735800

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
National University of Ireland, Galway, Ireland
Registry
ClinicalTrials.gov
Start date
18 October 2024
Est. completion
1 February 2027

Where this trial is recruiting

🇮🇪 Ireland

Primary endpoints

Reduction in re-admission rates

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: 22 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