search
Back to results

Dietary Supplements for COVID-19

Primary Purpose

Covid19

Status
Terminated
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Vitamin D3 50,000 IU
Vitamin C/Zinc
Vitamin K2/D
Microcrystalline Cellulose Capsule
Medium Chain Triglyceride Oil
Sponsored by
The Canadian College of Naturopathic Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19 focused on measuring Natural Health Products, NHP, Dietary Supplements, Vitamin C, Vitamin D, Vitamin K, Zinc, COVID-19, SARS-CoV-2

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Adults (≥18) who test positive for SARS-CoV-2 in an outpatient setting
  2. Access to internet

Exclusion Criteria:

  1. Symptom onset greater than 4 days prior to enrolment
  2. Supplementing regularly with >500 mg vitamin C, >1000 units vitamin D, >120 mcg vitamin K (any form), or >15 mg zinc taken daily within the past month
  3. Currently taking warfarin or an equivalent vitamin K antagonist anticoagulant
  4. End stage chronic kidney disease
  5. History of calcium oxalate kidney stones
  6. Active granulomatosis (sarcoidosis, tuberculosis, lymphoma)
  7. Known hypercalcemia or hypervitaminosis D
  8. Currently taking either of the following antibiotics: cephalexin, tetracyclines
  9. Participating in an investigational study or participation in an investigational study within the past 30 days
  10. Any reason which, under the discretion of the qualified investigator or delegate, would preclude the patient from participating.

Sites / Locations

  • The Centre for Health Innovation

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Treatment

Control

Arm Description

Specific Product: Vitamin D3 50,000 IU Formulation: Capsule. Each capsule will contain 500 mg (50,000 units) cholecalciferol (vitamin D3) Dose: One capsule on day 1 of the intervention period Specific Product: Vitamin K2/D Formulation: Liquid. Each 0.0285 mL drop contains 30 mcg menaquinone-7 (MK-7, vitamin K2) and 3.125 mcg (125 units) cholecalciferol (vitamin D3). Dose: 0.114 mL (four drops) twice daily for 21 days totalling 240mcg MK-7 and 1,000 units cholecalciferol per day. Specific Product: Vitamin C/Zinc Formulation: Capsule. Each capsule will contain 666 mg ascorbic acid (vitamin C) and 8.3 mg of zinc acetate Dose: Three capsules three times daily for 21 days totalling 6 g ascorbic acid and 75 mg zinc acetate per day.

Specific Product: Vitamin D3 50,000 IU Placebo Equivalent: microcrystalline cellulose capsule, 350 mg Specific Product: Vitamin K2/D Placebo Equivalent: Medium chain triglyceride oil Specific Product: Vitamin C/Zinc Placebo Equivalent: microcrystalline cellulose capsule, 350 mg

Outcomes

Primary Outcome Measures

Participant-reported overall health
Measured using the EuroQol Visual Assessment Scale (EQ-VAS). Scores each day range from 0 (worst health imaginable) and 100 (best health imaginable).

Secondary Outcome Measures

Effect of COVID-19 on the health status of participants
Measured using the EuroQol 5-Dimension 5-Level (EQ-5D-5L) questionnaire. Scores are converted into a unique health state. Health states are converted to an index value between 0 and 1, where 1 is considered the best possible health.
Symptom Severity of common COVID-19 symptoms
Measured using an internally-developed questionnaire. Includes fever, cough, shortness of breath, fatigue, headache, myalgia/arthralgia, nausea, vomiting, diarrhea, congestion, loss of taste, and loss of smell. Scores range from 0-3 for each symptom, totaling 0-42 for each day. 0 = no symptom, 1 = mild symptom, 2 = moderate symptom, 3 = severe symptom.
Total symptom duration
Measured as the time to a complete reduction of symptoms with no relapses (i.e., a 0 in all categories on the symptom questionnaire).
Incidence of delayed return to usual health
Measured by the number of people experiencing "ongoing symptomatic COVID-19" (symptoms persisting between 4 and 12 weeks) and the number of people experiencing "post-COVID-19 syndrome" (symptoms persisting longer than 12 weeks)
Frequency of Hospitalizations
Includes ER visits, acute care admissions, and ICU admissions
Hospital Length of Stay
Number of days in acute care or ICU
All-cause mortality

Full Information

First Posted
March 1, 2021
Last Updated
October 21, 2022
Sponsor
The Canadian College of Naturopathic Medicine
Collaborators
Ottawa Hospital Research Institute, Vitazan Professional, New Roots Herbal
search

1. Study Identification

Unique Protocol Identification Number
NCT04780061
Brief Title
Dietary Supplements for COVID-19
Official Title
Dietary Supplements to Reduce Symptom Severity and Duration in People With SARS-CoV-2: A Randomized, Double Blind, Placebo Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Terminated
Why Stopped
Public PCR testing stopped in Ontario
Study Start Date
July 12, 2021 (Actual)
Primary Completion Date
May 3, 2022 (Actual)
Study Completion Date
July 7, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Canadian College of Naturopathic Medicine
Collaborators
Ottawa Hospital Research Institute, Vitazan Professional, New Roots Herbal

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a double blind, placebo controlled, phase III randomized controlled trial evaluating the effects of the dietary supplements vitamin C, vitamin D, vitamin K, and zinc versus placebo on the overall health, symptom severity, and symptom duration of outpatients diagnosed with SARS-CoV-2.
Detailed Description
This study proposed is a double-blind, placebo-controlled, phase III randomized controlled trial powered to detect meaningful differences in the overall health and symptom severity of people with COVID-19 between the treatment and control arms. Eligible participants will be randomly assigned, using a web randomization system, in a ratio of 1:1 to one of the following groups: (1) nutrient therapy with vitamin D, vitamin C, vitamin K2, and zinc or (2) placebo. Total trial duration will be 12 weeks. Nutrients or placebo will be given for a period of 21 days following enrolment and randomization. Total trial duration will be 12 weeks. Adverse events will be collected during the treatment phase plus one additional week (maximum 4 weeks). With respect to the primary outcome of participant-reported overall health, power calculations were conducted based on between-group differences at a single time point (21 days) and Cohen's guideline for a small effect size of 0.3. A sample size of 176 (88 per arm) provides 80% power to detect a difference at an α of 0.05. To account for an approximate 10-15% lost to follow-up we will enrol 200 participants (100 per arm).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19
Keywords
Natural Health Products, NHP, Dietary Supplements, Vitamin C, Vitamin D, Vitamin K, Zinc, COVID-19, SARS-CoV-2

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
Specific Product: Vitamin D3 50,000 IU Formulation: Capsule. Each capsule will contain 500 mg (50,000 units) cholecalciferol (vitamin D3) Dose: One capsule on day 1 of the intervention period Specific Product: Vitamin K2/D Formulation: Liquid. Each 0.0285 mL drop contains 30 mcg menaquinone-7 (MK-7, vitamin K2) and 3.125 mcg (125 units) cholecalciferol (vitamin D3). Dose: 0.114 mL (four drops) twice daily for 21 days totalling 240mcg MK-7 and 1,000 units cholecalciferol per day. Specific Product: Vitamin C/Zinc Formulation: Capsule. Each capsule will contain 666 mg ascorbic acid (vitamin C) and 8.3 mg of zinc acetate Dose: Three capsules three times daily for 21 days totalling 6 g ascorbic acid and 75 mg zinc acetate per day.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Specific Product: Vitamin D3 50,000 IU Placebo Equivalent: microcrystalline cellulose capsule, 350 mg Specific Product: Vitamin K2/D Placebo Equivalent: Medium chain triglyceride oil Specific Product: Vitamin C/Zinc Placebo Equivalent: microcrystalline cellulose capsule, 350 mg
Intervention Type
Drug
Intervention Name(s)
Vitamin D3 50,000 IU
Other Intervention Name(s)
Cholecalciferol
Intervention Description
This is a loading dose of Vitamin D. Vitamin D (cholecalciferol [vitamin D3]) is a fat-soluble vitamin that is synthesized following ultraviolet radiation to the skin, naturally occurs in a few dietary sources and is available as a dietary supplement.
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin C/Zinc
Intervention Description
This is a combination of Vitamin C and Zinc. Vitamin C (ascorbic acid, ascorbate) is a water-soluble vitamin that naturally occurs in many foods and is sold as a dietary supplement. It is required for the functioning of several enzymes and is important for the immune system. Zinc is one of the most abundant essential trace elements in the human body and is required for the function of several hundred enzymes and transcription factors.
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin K2/D
Intervention Description
This is a combination of Vitamin K2 (menaquinone-7) and vitamin D. Vitamin K (menaquinone-7 [vitamin K2]) is a fat-soluble vitamin found in foods and sold as a dietary supplement. Vitamin K plays a large role in synthesizing coagulation factors in the blood, and vitamin K deficiency has been associated with uncontrolled bleeding. Vitamin K1 (phylloquinone) is an alternate form of vitamin K found in foods and supplements; however, vitamin K2 has a better absorption profile50 and additionally plays a role in bone metabolism controlling the binding of calcium, especially in older adults, where it attenuates the rate of bone loss
Intervention Type
Other
Intervention Name(s)
Microcrystalline Cellulose Capsule
Intervention Description
Placebo equivalent of Vitamin C/Zinc and Vitamin D3.
Intervention Type
Other
Intervention Name(s)
Medium Chain Triglyceride Oil
Intervention Description
Placebo equivalent of Vitamin K2/D
Primary Outcome Measure Information:
Title
Participant-reported overall health
Description
Measured using the EuroQol Visual Assessment Scale (EQ-VAS). Scores each day range from 0 (worst health imaginable) and 100 (best health imaginable).
Time Frame
During the intervention period (Daily for 21 days)
Secondary Outcome Measure Information:
Title
Effect of COVID-19 on the health status of participants
Description
Measured using the EuroQol 5-Dimension 5-Level (EQ-5D-5L) questionnaire. Scores are converted into a unique health state. Health states are converted to an index value between 0 and 1, where 1 is considered the best possible health.
Time Frame
Baseline plus weeks 1, 2, 3, 4, 8, and 12
Title
Symptom Severity of common COVID-19 symptoms
Description
Measured using an internally-developed questionnaire. Includes fever, cough, shortness of breath, fatigue, headache, myalgia/arthralgia, nausea, vomiting, diarrhea, congestion, loss of taste, and loss of smell. Scores range from 0-3 for each symptom, totaling 0-42 for each day. 0 = no symptom, 1 = mild symptom, 2 = moderate symptom, 3 = severe symptom.
Time Frame
During the intervention period (Daily for 21 days)
Title
Total symptom duration
Description
Measured as the time to a complete reduction of symptoms with no relapses (i.e., a 0 in all categories on the symptom questionnaire).
Time Frame
During the intervention period (21 days)
Title
Incidence of delayed return to usual health
Description
Measured by the number of people experiencing "ongoing symptomatic COVID-19" (symptoms persisting between 4 and 12 weeks) and the number of people experiencing "post-COVID-19 syndrome" (symptoms persisting longer than 12 weeks)
Time Frame
12 weeks
Title
Frequency of Hospitalizations
Description
Includes ER visits, acute care admissions, and ICU admissions
Time Frame
12 weeks
Title
Hospital Length of Stay
Description
Number of days in acute care or ICU
Time Frame
12 weeks
Title
All-cause mortality
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults (≥18) who test positive for SARS-CoV-2 in an outpatient setting Access to internet Exclusion Criteria: Symptom onset greater than 4 days prior to enrolment Supplementing regularly with >500 mg vitamin C, >1000 units vitamin D, >120 mcg vitamin K (any form), or >15 mg zinc taken daily within the past month Currently taking warfarin or an equivalent vitamin K antagonist anticoagulant End stage chronic kidney disease History of calcium oxalate kidney stones Active granulomatosis (sarcoidosis, tuberculosis, lymphoma) Known hypercalcemia or hypervitaminosis D Currently taking either of the following antibiotics: cephalexin, tetracyclines Participating in an investigational study or participation in an investigational study within the past 30 days Any reason which, under the discretion of the qualified investigator or delegate, would preclude the patient from participating.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dugald Seely, ND, MSc
Organizational Affiliation
Canadian College of Naturopathic Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kumanan Wilson, MD, MSc
Organizational Affiliation
The Ottawa Hospital Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Centre for Health Innovation
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K2P0M7
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35241474
Citation
Legacy M, Seely D, Conte E, Psihogios A, Ramsay T, Fergusson DA, Kanji S, Simmons JG, Wilson K. Dietary supplements to reduce symptom severity and duration in people with SARS-CoV-2: study protocol for a randomised, double-blind, placebo controlled clinical trial. BMJ Open. 2022 Mar 3;12(3):e057024. doi: 10.1136/bmjopen-2021-057024.
Results Reference
derived

Learn more about this trial

Dietary Supplements for COVID-19

We'll reach out to this number within 24 hrs