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NCT07206875Recruiting

Observational Study for the Characterisation of Patients Affected by Any Type of Diabetes and Endocrine Disorders

Retrospective and Prospective Observational Registry for the Characterisation of Patients Affected by Any Type of Diabetes and Endocrine-metabolic Disorders

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

The main objective of this retrospective and prospective observational register is to identify anthropometric, clinical, laboratory and/or instrumental markers of disease severity and activity in patients suffering from diabetes, endocrine-metabolic disorders, rare diseases in order to improve their diagnosis, monitoring and treatment processes. The Registry is monocentric, observational prospective and retrospective. No additional procedures to those of normal clinical practice are planned, and neither diagnostic approaches nor experimental drugs/prescriptions will be applied. The data under study (demographic, anthropometric, clinical and care characteristics) will be collected as part of outpatient visits of the Diabetes Outpatient Clinic or admission to Diabetes Day Hospital. In case of outpatients, the observation will start at the diagnosis or during the first outpatient visit and will end with the last outpatient visit performed within the total time foreseen for the duration of the study. The study will start once the regulatory authorizations are completed, and is expected to last at least 10 years with the possibility of extension

Status (registry)
Recruiting
Study type
Observational
Enrollment
10000 (estimated)
First submitted
23 Jul 2025
Start date
3 Nov 2025
Primary completion date
Nov 2026
Lead sponsor
IRCCS San Raffaele
NCT number
NCT07206875

What you commit to

  • Study type: Observational
  • Planned participants: 10000
  • From 3 Nov 2025 to the primary completion date, Nov 2026
  • 1 site in 1 country
  • 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.

Age

  • Age \<18 years

Other

  • Deny participation at the study
  • Recruitment in an interventional protocol
  • Patients with missing significant data

Who the study is looking for

  • Age ≥18 years
  • Outpatient Diabetes Unit patient
  • Ability to give informed consent
    • Diagnosis of at least one of the following:
  • Metabolic disease, defined as BMI ≥25 Kg/m2
  • Type 1 or type 2 diabetes mellitus
  • Gestational diabetes
  • Monogenic diabetes (MODY)
  • Other types of diabetes or dysglycemia
  • Dyslipidemia
  • Arterial hypertension
  • Steatosis liver disease (SLD)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Diabetology Department, San Raffaele Scientific Institute
Coordinator of this site? Confirm its status
MilanItalyRecruiting

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