Severity of COVID-19 and Vitamin D Supplementation
Primary Purpose
COVID-19 Respiratory Infection
Status
Active
Phase
Phase 4
Locations
Russian Federation
Study Type
Interventional
Intervention
vitamin D
Sponsored by
About this trial
This is an interventional treatment trial for COVID-19 Respiratory Infection focused on measuring level of 25-hydroxyvitamin, 25(OH)D, vitamin D, COVID-19, treatment, prevention
Eligibility Criteria
Inclusion Criteria:
- males and females aged 18 to 75 years
- who did not take Vitamin D supplementation
- COVID-19 clinical features
- signed informed consent to participate in the research.
Exclusion Criteria:
- pregnancy or nursing
- primary hyperparathyroidism or hypercalcemia other etiologies (including 24-hydroxylase mutation)
- a history of granulomatous diseases
- severe gastrointestinal diseases (clinically apparent malabsorption syndrome)
- liver disease
- kidney disease
- individual intolerance drug
- vitamin D supplementation in a dose of more than 800 IU per
- drugs known to affect vitamin D metabolism (e.g., anticonvulsants, glucocorticoids, diuretics)
- alcohol and drug addiction.
- history of cancer (less than 5 years)
Sites / Locations
- Almazov National Medical Research Centre, of the Ministry of Health of the Russian Federation
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
High dose
Low dose
Arm Description
High dose Vitamin D therapy will initiate at a dosage of 50,000 IU on the first and second week of hospitalization
Vitamin D therapy will prescribe at a dosage of 2,000 IU/day
Outcomes
Primary Outcome Measures
Combined: severity, ICU hospitalization, outcome of the disease on 14-21 days
Severity of new coronavirus infection- moderate, severe, extremely severe
Hospitalization in intensive care unit
Outcome of the disease - recovery or fatal outcome
Secondary Outcome Measures
Serum 25(OH)D level
Serum APPs (acute phase proteins) levels, cytokine/chemokine concentrations
Change in the serum concentration of CRP (C-reactive protein), ferritin, LDH (lactate dehydrogenase), IL-6
Duration of hospitalization
number of days spent in hospital
Interleukin-6 inhibitors application
The need to use Interleukin-6 Inhibitors - olokizumab, tocilixamab, levilimab
Full Information
NCT ID
NCT05166005
First Posted
December 12, 2021
Last Updated
December 20, 2021
Sponsor
Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health
1. Study Identification
Unique Protocol Identification Number
NCT05166005
Brief Title
Severity of COVID-19 and Vitamin D Supplementation
Official Title
The Effect of Vitamin D Supplementation in Standard Therapy on Reducing Severity of COVID-19 Among Hospitalized Patients
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 1, 2020 (Actual)
Primary Completion Date
August 23, 2021 (Actual)
Study Completion Date
December 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Purpose of the study: to analyze the interlinks between serum 25(OH)D level and severity of new coronavirus infection (COVID-19) in hospitalized patients, as well as the effect of adding colecaciferol to standard therapy for patients in the acute period of the disease.
The study will involve at least 300 hospitalized patients with confirmed COVID-19. All study participants will be twice assessed for serum 25 (OH) D levels: baseline and 8-10 days of hospitalization. Following a baseline examination, patients will be randomized into 2 groups. Group I (No. 1), vitamin D therapy begins with a dosage of 50,000 IU in the first and second weeks. Group II (No. 2), vitamin D therapy is prescribed at a dosage of 2000 IU / day. On 8-10 days of vitamin D supplementation, all participants will be retested for serum 25 (OH) D levels to assess the effectiveness of therapy. On 14-21 days we assessed severity of the course, ICU hospitalization, duration of hospitalization, outcome of the disease, duration of glucocorticoid therapy, the need for specific therapy (inhibitors IL-6), changes in cytokine/chemokine, APPs concentration.
Detailed Description
The COVID-19 pandemic that swept the world in 2019 radically changed not only the social sphere of life, subordinating everything around to its influence, but also the healthcare sector. It affected both its practical and scientific sides, globally changing the approach to medicine. Numerous studies around the globe are being conducted on the prevention and treatment of this infection. A significant amount of them study the role of vitamin D in the pathogenesis of the disease. Cholecalciferol (Vitamin D) is a fat-soluble vitamin that is involved in maintaining the serum calcium-phosphorus gradient. Vitamin D supplementation significantly reduces the risk of osteoporosis, and also affects the regulation of immune responses by modulating innate and adaptive immune responses. It has been shown to inhibit the proliferation of T cells, namely the subsequent transformation of Th1 cells to Th2 cells. This effect on cell proliferation and differentiation contributes to a significant decrease in the level of proinflammatory cytokines, thereby reducing the severity of immune-mediated damage. It was these mechanisms that formed the basis of the theory about the ability of vitamin D to prevent the severe course of coronavirus infection and even prevent it. At the moment, the effect of vitamin D on reducing COVID-19 morbidity is not fully confirmed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19 Respiratory Infection
Keywords
level of 25-hydroxyvitamin, 25(OH)D, vitamin D, COVID-19, treatment, prevention
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
350 (Actual)
8. Arms, Groups, and Interventions
Arm Title
High dose
Arm Type
Active Comparator
Arm Description
High dose Vitamin D therapy will initiate at a dosage of 50,000 IU on the first and second week of hospitalization
Arm Title
Low dose
Arm Type
Placebo Comparator
Arm Description
Vitamin D therapy will prescribe at a dosage of 2,000 IU/day
Intervention Type
Drug
Intervention Name(s)
vitamin D
Intervention Description
Patients will be randomised to receive either high dose vitamin D (50,000 IU weekly) on the first and second week or low dose vitamin D (2,000 IU daily).
Primary Outcome Measure Information:
Title
Combined: severity, ICU hospitalization, outcome of the disease on 14-21 days
Description
Severity of new coronavirus infection- moderate, severe, extremely severe
Hospitalization in intensive care unit
Outcome of the disease - recovery or fatal outcome
Time Frame
baseline and on 14-21 days
Secondary Outcome Measure Information:
Title
Serum 25(OH)D level
Time Frame
baseline and on 9-10 days
Title
Serum APPs (acute phase proteins) levels, cytokine/chemokine concentrations
Description
Change in the serum concentration of CRP (C-reactive protein), ferritin, LDH (lactate dehydrogenase), IL-6
Time Frame
baseline and on 14-21 days
Title
Duration of hospitalization
Description
number of days spent in hospital
Time Frame
baseline and on 14-21 days
Title
Interleukin-6 inhibitors application
Description
The need to use Interleukin-6 Inhibitors - olokizumab, tocilixamab, levilimab
Time Frame
baseline and on 14-21 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
males and females aged 18 to 75 years
who did not take Vitamin D supplementation
COVID-19 clinical features
signed informed consent to participate in the research.
Exclusion Criteria:
pregnancy or nursing
primary hyperparathyroidism or hypercalcemia other etiologies (including 24-hydroxylase mutation)
a history of granulomatous diseases
severe gastrointestinal diseases (clinically apparent malabsorption syndrome)
liver disease
kidney disease
individual intolerance drug
vitamin D supplementation in a dose of more than 800 IU per
drugs known to affect vitamin D metabolism (e.g., anticonvulsants, glucocorticoids, diuretics)
alcohol and drug addiction.
history of cancer (less than 5 years)
Facility Information:
Facility Name
Almazov National Medical Research Centre, of the Ministry of Health of the Russian Federation
City
Saint Petersburg
ZIP/Postal Code
194021
Country
Russian Federation
12. IPD Sharing Statement
Learn more about this trial
Severity of COVID-19 and Vitamin D Supplementation
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