Actively Recruiting
Prospective Monocentric Registry of Patients Undergoing Vitamin D Treatment at San Raffaele Hospital
Led by IRCCS San Raffaele · Updated on 2026-04-08
1000
Participants Needed
1
Research Sites
256 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers at the Endocrinology Unit of the IRCCS San Raffaele Hospital are establishing a prospective, single-center registry to collect data on patients undergoing vitamin D supplementation. The study focuses on patients with hypovitaminosis D and aims to assess epidemiological trends, identify risk factors, and evaluate current diagnostic and treatment approaches. This observational study will track patients' clinical progress over ten years. Participants will receive vitamin D supplementation according to standard clinical care, without experimental interventions, as the study uses an observational design. The registry will collect data from outpatient visits to the Endocrinology Unit, including clinical, laboratory, and historical information, following usual diagnostic and treatment protocols for endocrine-metabolic diseases. During the study, researchers will monitor changes from baseline in patients receiving vitamin D over a period of ten years. Participants will have regular outpatient visits where their health status and treatment effects will be recorded. The study aims to provide long-term insights into managing hypovitaminosis D and will continue data collection until December 2034.
CONDITIONS
Brief Title
Prospective Monocentric Registry of Patients Undergoing Vitamin D Treatment at San Raffaele Hospital
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult men and women aged 18 years or older, regardless of fertility, pregnancy, or breastfeeding status
- Currently receiving vitamin D supplementation of any formulation or dosage
- Able to understand and sign informed consent
You will not qualify if you...
- Patients unable to understand or sign informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 10 years
Participants who are receiving vitamin D supplementation are observed over time to assess changes in their health data.
Outpatient visits as part of routine endocrinology care
Trial Site Locations
Total: 1 location
1
IRCCS Ospedale San Raffaele
Milan, Italy, 20132
Actively Recruiting
Research Team
L
Luigi Di Filippo, MD
E
Endocrinology Trial Office, CRN
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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