Describing the Clinical-laboratory Aspects of Diabetes Through the Creation of a Registry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Diabetes. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Italy
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Describing the Clinical-laboratory Aspects of Diabetes by Creating a Registry in Which to Census All Newly Diagnosed or Already Diagnosed Cases After 1/1/2000 at the Endocrinology and Diabetes Prevention and Treatment Unit
Overview
The main objective of the study is to describe the clinical-laboratory aspects of diabetes by creating a registry in which to census all newly diagnosed or already diagnosed cases after 1/1/2000 at the O.U. of Endocrinology and Diabetes Prevention and Care.
Detailed description
The main objective of the study is to describe the clinical-laboratory aspects of diabetes by creating a registry in which to census all newly diagnosed or already diagnosed cases after 1/1/2000 at the O.U. of Endocrinology and Diabetes Prevention and Care.
The clinical-laboratory aspects covered by this study also include family history, survival, comorbidities, psychological aspects, and in any case all those data that add relevant scientific information. This registry may be used to review the OU's case history and to confirm or obtain new scientific evidence on diabetes through cohort studies conducted using the data that will be recorded.
Primary outcome measures
- Clinical-Laboratory Aspects of Diabetes - Family History [Time frame: through study completion, an average of 26 years]
- Clinical-Laboratory Aspects of Diabetes - Survival [Time frame: through study completion, an average of 26 years]
- Clinical-Laboratory Aspects of Diabetes - Comorbidities [Time frame: through study completion, an average of 26 years]
- Psychological Factors in Diabetes Management: Depression, Anxiety, and Quality of Life [Time frame: through study completion, an average of 26 years]
- Blood Glucose and HbA1c Levels in Diabetes [Time frame: through study completion, an average of 26 years]
- Aggregated Data on Diabetes Progression and Management [Time frame: through study completion, an average of 26 years]
- Lipid Profile in Diabetes [Time frame: through study completion, an average of 26 years]
- Kidney Function Tests in Diabetes [Time frame: through study completion, an average of 26 years]
Eligibility criteria
Inclusion criteria
- Age >18 years
- Newly or previously diagnosed patients with diabetes mellitus at any stage of disease
- Obtaining informed consent
Exclusion criteria
\- Patients whose diagnosis of diabetes mellitus is uncertain
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
Italy · 1 center
- IRCCS Azienda Ospedaliero-Universitaria di Bologna — Bologna
Identifiers
NCT: NCT06797947 · REDIA