Fact CheckerSign in

NCT05705869Active, not recruiting

Targeted Assessment in High-Risk paTients With dIAbetes to ideNtify Undiagnosed Heart Failure

Targeted Assessment in High-Risk paTients With dIAbetes to ideNtify Undiagnosed Heart Failure (TARTAN-HF)

Source: ClinicalTrials.gov · Last updated 14 Jan 2026

Brief summary (registry, in English)

This is a prospective, multicentre, unblinded, randomised, controlled trial. The primary aim is to assess a targeted screening strategy to detect undiagnosed heart failure in high-risk patients with diabetes.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
706 (actual)
First submitted
21 Dec 2022
Start date
22 Dec 2022
Primary completion date
30 Nov 2025
Lead sponsor
NHS Greater Glasgow and Clyde
NCT number
NCT05705869

What you commit to

  • Study type: Interventional
  • Participants enrolled: 706
  • From 22 Dec 2022 to the primary completion date, 30 Nov 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous documented diagnosis of heart failure.
  • Currently receiving scheduled renal replacement therapy.

Other illness

  • Inability to give informed consent e.g., due to significant cognitive impairment.
  • Echocardiogram or NT-proBNP interpreted as excluding heart failure within 12 months.

Other

  • Anyone who, in the investigators' opinion, is not suitable to participate in the trial for other reasons e.g., a diagnosis which may compromise survival over the study period

Who the study is looking for

  • Male or female ≥40 years of age
  • Informed consent
  • An established diagnosis of diabetes (type 1 or type 2)
  • At least one additional risk factor for heart failure:
    • Coronary artery disease (either a previous documented type 1 myocardial infarction or coronary artery bypass grafting or percutaneous coronary intervention or documented stenosis of an epicardial coronary artery \[\>50% left main or \>70% left anterior descending, circumflex or right coronary artery\])
    • Persistent or permanent atrial fibrillation (not paroxysmal atrial fibrillation)
    • Previous ischemic or embolic stroke
    • Peripheral arterial disease (previous surgical or percutaneous revascularisation or a documented stenosis greater than 50% of a major peripheral arterial vessel).
    • Chronic kidney disease (defined as an estimated glomerular filtration rate \<60mL/min/1.73m2 or eGFR 60-90mL/min/1.73m2 and UACR \>300mg/g).
    • Regular loop diuretic use (any dose at any dosing interval) for \>30 days.
    • COPD (evidenced by one of the following; PFTs showing airway obstruction, diagnosis by respiratory physician, CT scan reporting presence of emphysema or treatment with national guideline-advocated COPD therapy).

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Glasgow Royal Infirmary
Coordinator of this site? Confirm its status
GlasgowUnited KingdomUnknown status
Queen Elizabeth University Hospital
Coordinator of this site? Confirm its status
GlasgowUnited KingdomUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.