The VITDALIZE Study: Effect of High-dose Vitamin D3 on 28-day Mortality in Adult Critically Ill Patients
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- COVID-19
- Critical Illness
- Vitamin D Deficiency
- Type
- Interventional
- Phase
- Phase 3
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Triple (Participant, Care Provider, Investigator)Primary Purpose: Treatment
Participation Requirements
- Age
- Between 18 years and 100 years
- Gender
- Both males and females
Description
A very limited number of intervention trials, most including less than 30 patients, have been published. The only phase III study, our VITdAL-ICU study recruited from 2010 to 2012 and (n=475) did not find a difference in the primary endpoint "length of hospital stay" between placebo and high-dose vi...
A very limited number of intervention trials, most including less than 30 patients, have been published. The only phase III study, our VITdAL-ICU study recruited from 2010 to 2012 and (n=475) did not find a difference in the primary endpoint "length of hospital stay" between placebo and high-dose vitamin D3. However, there was a non-significant absolute risk reduction in all-cause hospital mortality in the total population. The difference was larger (17.5%) and significant in the predefined subgroup of patients with severe vitamin D deficiency at baseline, see Kaplan Meier curve below (n=200, 28.6 vs 46.1%, p=0.01, 0.56 (0.35-0.90) ), corresponding to a number needed to treat of 6. (51) As this was only a secondary endpoint in the predefined subgroup with severe vitamin D deficiency, this finding is hypothesis generating and requires further study, leading to this application. In our study, we were unable to identify a mechanism by which this benefit was achieved. Interestingly, looking at the causes of death, the vitamin D group seemed to benefit in every category. The VITDALIZE study is a pragmatic, multicenter, placebo-controlled double-blind randomized controlled phase III trial in adult critically ill patients which will be conducted in academic and non-academic centers. The sponsor is the Medical University of Graz, Austria. Subjects will be randomised in a 1:1 ratio to receive either of the two treatments: Vitamin D: oral/enteral pharmacological dose of cholecalciferol (vitamin D3) total dose 900,000 loading dose of 540,0000 (dissolved in 37.5 ml of medium chain triglycerides - MCT) followed by 4000 IU daily (10 drops) for the entire active study period (90 days) Placebo: identical regime - loading dose of 37.5 ml MCT followed by 10 drops daily This study uses a group sequential design, with one interim analysis when 50% of the planned enrolled patients in each arm (N=600 per arm) have completed their day 28 assessment by the independent data safety monitoring board. The enrollment of patients will continue while the interim analyses is performed.
Tracking Information
- NCT #
- NCT03188796
- Collaborators
- Krankenhaus Barmherzige Schwestern Linz
- Medical University of Vienna
- Medical University Innsbruck
- Hospital Barmherzige Brüder St. Veit
- Klinikum Klagenfurt am Wörthersee
- Johannes Kepler University of Linz
- Barmherzige Brüder Vienna
- Erasme University Hospital
- Wuerzburg University Hospital
- University of Birmingham
- Centre Hospitalier Régional de la Citadelle
- Centre Hospitalier Universitaire de Charleroi
- University Hospital, Frankfurt
- Kages
- KABEG Management
- Centre Hospitalier Universitaire Mons
- Investigators
- Principal Investigator: Karin Amrein, MD, MSc Medical University of Graz