Global registry for patients with type 2 diabetes and related conditions

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational registry aims to collect real-world data on patient characteristics, disease management, healthcare utilization, and outcomes for individuals with type 2 diabetes, hypertension, heart failure, and chronic kidney disease. It will utilize a cloud-based electronic case report form (eCRF) for both prospective and retrospective data collection, making it accessible to investigators and a Scientific Committee. The registry is open to physicians worldwide who manage these conditions, facilitating a comprehensive understanding of patient care in clinical practice.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Being 18 years or older
2. Having type 2 diabetes, Hypertension, Heart Failure and/or chronic kidney disease
3. Providing written informed consent to participate in the registry

Exclusion Criteria:

1. Having a life-threatening co-morbidity with life expectancy below 1 year
2. Participating in an interventional trial requiring informed consent

Where it's running

• Research Site
  Fortaleza, Ceará, Brazil Recruiting
• Research Site
  Colatina, Espírito Santo (ES), Brazil Recruiting
• Research Site
  Salvador, Estado de Bahia, Brazil Recruiting
• Research Site
  Brasília, Federal District, Brazil Recruiting
• Research Site
  Poços de Caldas, Minas Gerais, Brazil Recruiting
• Research Site
  Campina Grande do Sul, Paraná, Brazil Recruiting

+26 more sites. See ClinicalTrials.gov for the full list.

Study contacts

• Study coordinator: AstraZeneca Clinical Study Information Center
• Email: information.center@astrazeneca.com
• Phone: 1-877-240-9479

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.