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Vitamin D Insufficiency inVestigation Among hospitaLizeD Inpatients

Vitamin D Insufficiency inVestigation Among hospitaLizeD Inpatients

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05214040
Acronym
VIVALDI
Enrollment
300000
Registered
2022-01-28
Start date
2022-09-30
Completion date
2026-09-30
Last updated
2022-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypovitaminosis D

Brief summary

Hypovitaminosis D is common in the adult population, it affects at least 1 billion people worldwide, and in particular 80% of the French population according to the National Institute for Public Health Surveillance. Hypovitaminosis D is accompanied or complicated by deleterious health manifestations such as bone, immune and cancer diseases, neuromuscular disorders and a propensity to fall, for example. Hypovitaminosis D has also been associated with more complicated care pathways (increase in the severity of the reason for hospitalization, length of hospitalization, risk of in-hospital death). Prevention of these clinical events depends on correcting vitamin D status. In sick, dependent or fragile adults, natural intakes are generally insufficient. It is indeed accepted that hypovitaminosis D may not be treated effectively by dietary measures or by simple exposure to the sun in French latitudes. Drug supplementation is therefore necessary, with the objective of achieving a target concentration of circulating 25-hydroxyvitamin D (25 (OH) D) of 75 nmol / L (30 ng / mL) in this population. Vitamin D supplementation, when properly conducted, corrects hypovitaminosis D, and has been associated with improved prognosis, especially life-saving, in therapeutic trials versus placebo. Such results lead the investigators to suggest that the identification and correction of hypovitaminosis D in hospitalized patients could represent a simple, effective and inexpensive strategy for improving hospital care pathways. In this perspective, the first step is to determine the prevalence, severity and clinical profile of hospitalized patients with hypovitaminosis D, as well as their course of care. To the investigators knowledge, there are no large-scale studies based on real-life data on this subject.

Interventions

None listed

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ≥ 18 years old * have had a dosage of circulating 25-hydroxyvitamin D (plasma or serum) in a HUGO establishment * consultant or hospitalized between 01/01/2015 and 12/31/2019 in one of the participating HUGOs.

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Prevalence and depth of hypovitaminosis Dbaselinethe prevalence of hypovitaminosis D will be calculated for each of the 3 definition thresholds for hypovitaminosis D found in the literature: ≤ 75 nmol/L, ≤ 50 nmol/L and ≤ 25 nmol/L.

Secondary

MeasureTime frameDescription
Clinical profilebaselineThe clinical profile will be determine by the data provided by the physician during the hospitalization or the consultation
Length of hospitalisationbaselinedetermine whether the circulating 25-hydroxyvitamin D concentration is associated with the length of hospitalization in days
Mortalitybaseline, 14 and 28 days, 3 and 6 months after the dosagedetermine whether the circulating 25-hydroxyvitamin D concentration is associated with the death occurring during hospital stay.

Contacts

Primary ContactCédric ANNWEILER, MD,PhD
cedric.annweiler@chu-angers.fr02 41 35 47 25

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026