Actively Recruiting
Swiss Diabetes Registry - SwissDiab Study
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2024-12-04
1500
Participants Needed
4
Research Sites
4643 weeks
Total Duration
On this page
Sponsors
I
Insel Gruppe AG, University Hospital Bern
Lead Sponsor
C
Cantonal Hospital of St. Gallen
Collaborating Sponsor
AI-Summary
What this Trial Is About
Currently, the estimated number of people with diabetes mellitus is approximately 387 million people worldwide. Due to population growth, urbanization, ageing and the rising prevalence of obesity the numbers of individuals with diabetes is increasing likewise. It has been shown that improving glycemic control is associated with a reduction in late complications of diabetes, such as cardiovascular and microvascular diseases. Therefore, treatment guidelines were established internationally by large and renowned associations and adopted by many countries. For Switzerland only sparse data exist on the actual implementation of such recommendations and on patient's well-being. The Swiss Diabetes Registry - SwissDiab Study is a prospective cohort study aiming at including and collecting data of virtually all patients regularly seen and treated at the study centers (≈ 500 patients each), irrespective of type, duration of diabetes or treatment . This allows the evaluation of diabetes treatment strategies at these centers. Furthermore, risk indicators for micro- and macrovascular complications, mortality as well as costs and quality of life will be assessed. Data will be recorded through an internet-based, electronic database specifically designed for this study. At a later perspective it is planned to extend data collection to general practitioner/family doctor networks in order to include a larger and more representative sample of patients with diabetes in Switzerland.
CONDITIONS
Official Title
Swiss Diabetes Registry - SwissDiab Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Diagnosis of diabetes mellitus according to ADA criteria
- Able and willing to provide informed consent
You will not qualify if you...
- Gestational diabetes mellitus
- Unable to give informed consent
- Legally incompetent or unable to comply with study conditions
- Significantly reduced life expectancy (less than 1 year)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
Universitätspoliklinik für Endokrinologie, Diabetologie und Klinische Ernährung, Inselspital Bern
Bern, Switzerland, 3010
Actively Recruiting
2
Service d'endocrinologie, diabétologie et métabolisme
Lausanne, Switzerland
Actively Recruiting
3
Klinik für Endokrinologie, Diabetologie, Osteologie und Stoffwechselerkrankungen, Kantonsspital St.Gallen
Sankt Gallen, Switzerland, 9007
Actively Recruiting
4
Klinik für Endokrinologie, Diabetologie und Klinische Ernährung, Universitätsspital Zürich
Zurich, Switzerland, 8091
Actively Recruiting
Research Team
M
Markus Laimer, PD Dr. med.
CONTACT
C
Christoph Stettler, Prof.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here