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Taking people in United KingdomNo phase

Studying heart failure and diabetes to compare how the body's tissues interact

Compares heart and metabolic tests in adults with heart failure, diabetes, or neither.

Plain-language title generated from the registry record
Registry title: Heart Failure in Patients With Diabetes: Cells, Crosstalk and Consequences

Key facts

Where
Leeds, United KingdomSee the site

Where in United Kingdom

  • Leeds Teaching Hospitals NHS TrustLeeds, United KingdomTaking people

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  4. What happens if I want to stop?
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Trial details

Who runs it
University of Leeds
Trial code
NCT06774014
Record updated
28 February 2025
Original description
This will be an observational study to explore differences in pathophysiology between groups of people with and without heart failure (HF) (reduced and preserved ejection fraction) and with and without diabetes mellitus (DM) with a particular focus on cross-talk (fat, muscle, vascular tissue and the heart). The investigators will invite 600 people to partcipate (100 with HFrEF+DM, 100 with HFpEF+DM, 100 with HFpEF-DM, 100 with HFrEF-DM, 100 with DM, 100 without either HR or DM). Special heart scans, exercise testing, blood testing, testing of the automatic nervous system will be performed and in some, samples of fat and muscle and endothelial cells will be collected.Read full original descriptionShow less

Heart Failure in Patients With Diabetes: Cells, Crosstalk and Consequences

This will be an observational study to explore differences in pathophysiology between groups of people with and without heart failure (HF) (reduced and preserved ejection fraction) and with and without diabetes mellitus (DM) with a particular focus on cross-talk (fat, muscle, vascular tissue and the heart). The investigators will invite 600 people to partcipate (100 with HFrEF+DM, 100 with HFpEF+DM, 100 with HFpEF-DM, 100 with HFrEF-DM, 100 with DM, 100 without either HR or DM). Special heart scans, exercise testing, blood testing, testing of the automatic nervous system will be performed and in some, samples of fat and muscle and endothelial cells will be collected.

These data will be used to create a cohort of well phenotyped patients with a variety of comprehensively collected clinical information, a cell atlas, and a comprehensive assessment of metabolomics, proeomics and cross-talk in between tissues, allowing comparisons between each group.

Inclusion: Age >18 years; Ability to provide written informed consent; Persons who are legally competent and mentally able to follow the instructions of the study staff.

Exclusion: Taking study medication (of an investigational drug) 30 days before the start of the study; Patients with acute infectious diseases (e.g. pneumonia); Patients with heart failure due to sepsis; People with acute myocardial ischemia, which is manifested, for example, by angina pectoris or ECG changes under stress; Patients with acute liver or kidney failure or severe COPD (FEV1<1.0); Anaemia Hb <8 mg/dl; Pregnant and breastfeeding women; People who are institutionalized on official or court orders; People who are dependent or employed by the sponsor or investigator.

ClinicalTrials.gov NCT06774014