DISCOVER iCaReMe Global Registry

  • End date
    Dec 31, 2025
  • participants needed
  • sponsor
Updated on 8 July 2021
heart failure


To provide real world data on patient characteristics, disease management, healthcare utilization, and outcomes in patients with type 2 diabetes, chronic kidney disease and heart failure


The registry intends to provide real world data on patient management and quality of care for patients with T2DM, heat failure and chronic kidney disease in clinical practice in many countries. To bridge this gap an observational voluntary registry is set up to capture real world data on patient characteristics, disease management, healthcare utilization, and outcomes in patients with type 2 diabetes, Heart Failure and Chronic Kidney Disease. Multinational, observational registry utilizing a cloud-based eCRF, for prospective and retrospective data collection, accessible to investigators and Scientific Committee. This registry will be open to all physicians managing T2DM, HF or CKD across the world.

Condition chronic renal insufficiency, NIDDM, Diabetes Mellitus, Chronic renal failure, Heart failure, Heart disease, Diabetes Mellitus, Type 2, Diabetes Prevention, Diabetes Mellitus Types I and II, Diabetes (Pediatric), Congestive Heart Failure, Diabetes Mellitus Type 2, chronic kidney disease, type 2 diabetes mellitus, chronic kidney disease (ckd), cardiac failure, type 2 diabetes, type ii diabetes, noninsulin-dependent diabetes mellitus, diabetes type 2, congestive heart disease
Clinical Study IdentifierNCT03549754
Last Modified on8 July 2021


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Inclusion Criteria

Being 18 years or older
Having type 2 diabetes, chronic kidney disease or heart failure
Providing written informed consent to participate in the registry

Exclusion Criteria

Having a life-threatening co-morbidity with life expectancy below 1 year
Participating in an interventional trial requiring informed consent
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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