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NCT05919342Recruiting

Screening for earlY Heart Failure Diagnosis and Management in Primary Care or at HOme Using Natriuretic Peptides and echocardiographY "SYMPHONY-HF"

Screening for earlY Heart Failure Diagnosis and Management in Primary Care or at HOme Using Natriuretic Peptides and echocardiographY

Source: ClinicalTrials.gov · Last updated 4 Aug 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is an international 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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
3904 (estimated)
First submitted
21 May 2023
Start date
22 Dec 2022
Primary completion date
21 Jun 2024
Lead sponsor
NHS Greater Glasgow and Clyde
NCT number
NCT05919342

What you commit to

  • Study type: Interventional
  • Planned participants: 3904
  • From 22 Dec 2022 to the primary completion date, 21 Jun 2024
  • 7 sites in 5 countries
  • 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
  • Current renal replacement therapy

Other illness

  • Inability to give informed consent e.g., due to significant cognitive impairment

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
  • Two or more of the following risk factors 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 \[50% left main stem or \>70% left anterior descending, circumflex or right coronary artery\])
    • An established diagnosis of diabetes (type 1 or type 2)
    • 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 (7)

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

SiteCityCountrySite status
University of Montreal
Coordinator of this site? Confirm its status
MontrealCanadaNot yet recruiting
University of British Columbia
Coordinator of this site? Confirm its status
VancouverCanadaNot yet recruiting
Rigshospitalet (Copenhagen University Hospital)
Coordinator of this site? Confirm its status
CopenhagenDenmarkNot yet recruiting
University of Glasgow
Coordinator of this site? Confirm its status
GlasgowUnited KingdomRecruiting
Karolinska University Hospital
Coordinator of this site? Confirm its status
StockholmSwedenNot yet recruiting
Uppsala University
Coordinator of this site? Confirm its status
UppsalaSwedenNot yet recruiting
Cleveland Clinic
Coordinator of this site? Confirm its status
ClevelandUnited StatesNot yet recruiting

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