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Coronavirus 2019 (COVID-19)- Using Ascorbic Acid and Zinc Supplementation

Coronavirus Disease 2019- Using Ascorbic Acid and Zinc Supplementation (COVIDAtoZ) Research Study A Randomized, Open Label Single Center Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04342728
Acronym
COVIDAtoZ
Enrollment
214
Registered
2020-04-13
Start date
2020-04-08
Completion date
2021-02-11
Last updated
2021-02-16

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

Conditions

COVID, Corona Virus Infection

Keywords

COVID-19, Viral Infection, Infection, Coronavirus-19, Ascorbic Acid, Zinc Gluconate

Brief summary

The purpose of this study is to examine the impact of ascorbic acid (vitamin c) and zinc gluconate in reducing duration of symptoms in patients diagnosed with coronavirus disease 2019 (COVID-19). Patients above the age of 18 who present to the Cleveland Clinic outpatient testing and receive a positive test for COVID-19 will be invited to participate.

Detailed description

We aim to see whether ascorbic acid and zinc gluconate which has limited side effect profile and is readily available over the counter can decrease the duration of symptoms seen in patients with new diagnosis of COVID-2019. A secondary purpose is to see whether Zinc and/or Ascorbic acid supplementation can prevent progression of the severe manifestations of the disease including development of dyspnea and acute respiratory distress syndrome which may require hospitalization, mechanical ventilation, and or lead to death. This is a single-center, prospective, randomized study which plans to enroll 520 patients with a principal diagnosis of COVID-2019, managed in an outpatient setting, who presented after being sent by a healthcare provider to get tested and receive a PCR (Polymerase Chain Reaction) -assay based confirmed diagnosis of the disease. All patients who agree to participate in the study will answer a baseline questionnaire about their symptoms at the time of inclusion. Patients will then be randomized to one of 4 study arms. Patients in Arm A (n=130) will receive vitamin C (to be taken divided over 2-3 times a day with meals), patients in Arm B (n=130) will receive zinc gluconate to be taken at bedtime, patients in Arm C (n=130) will receive both vitamin C (to be taken divided over 2-3 times a day with meals) and zinc gluconate (taken at bedtime). Patients in arms A, B and C will take study supplements daily for 10 days. Patients in Arm D (n=130) will not receive any of the study medications and continue on standard of care. Patients will then track their symptoms daily from day 0 to day 28 answering 12 basic questions on illness severity.They will stop filling out their daily questions once they reach reach the end of the 28 day study period or at time of hospitalization; whichever comes first . Study team members will call patients at days 7, 14, 21, and 28 of the study period to assess need for hospitalization, ER visit, or additional medications prescribed by a healthcare provider, and any side effects from the supplements that the patient could have experienced.

Interventions

DIETARY_SUPPLEMENTAscorbic Acid

Readily available marketed open label ascorbic acid

DIETARY_SUPPLEMENTZinc Gluconate

Readily available marketed open label zinc gluconate

DIETARY_SUPPLEMENTAscorbic Acid and Zinc Gluconate

Readily available marketed open label ascorbic acid and zinc gluconate

OTHERStandard of Care

Readily available prescribed medications/ supplements- None study supplements

Sponsors

The Cleveland Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

A single-center, prospective, open label four arm study (1. Zinc only 2. Zinc and ascorbic acid 3. Ascorbic acid only 4. Standard of care.

Eligibility

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

Inclusion criteria

* Outpatients ≥ 18 years presenting to Cleveland Clinic Health System in Ohio and Florida who test positive for COVID-19 having any of the following symptoms 1. Fever or chills 2. Shortness of breath or difficulty breathing 3. Cough 4. Fatigue 5. Muscle or body Aches 6. Headache 7. New loss of taste 8. New loss of smell 9. Congestion or runny nose 10. Nausea 11. Vomiting 12. Diarrhea Women of child bearing potential: 1. have had a menstrual period within the past 30 days, or 2. have had previous sterilization, or 3. are perimenopausal (less than 1 year) who have a negative pregnancy test, or 4. women of childbearing potential who do not meet the above and have a negative pregnancy test.

Exclusion criteria

* Patients who are found to be positive during hospitalization * Patients who reside outside Ohio or Florida. * Pregnant women: 1. Current known pregnancy 2. Positive pregnancy test (women of child bearing potential who have not had previous sterilization as defined as hysterectomy or tubal ligation) * Women of childbearing potential who do not meet the above criteria, last menstrual period greater than 30 days and have a positive pregnancy test. * Lactating Women * End stage kidney disease * Advanced liver disease awaiting transplant * History of Calcium Oxalate kidney stones.

Design outcomes

Primary

MeasureTime frameDescription
Symptom Reduction28 daysNumber of days to reach a 50 percent reduction in the cumulative 0-36 symptom score with each symptom evaluated on a 0-3 scale. Assessed symptoms are Fever, Cough, Shortness of Breath, Fatigue, Muscle or body aches, Headache, New loss of taste, New loss of smell, Congestion or runny nose, Nausea, Vomiting, Diarrhea. Each patient will have a composite score ranging from 0-36/day

Secondary

MeasureTime frameDescription
Symptom Resolution: Cough28 daysThe number of days required to reach a score of 0 from the symptom category of cough based on a 0-3 scale: 0 = no cough, 1 = mild, 2 = moderate, 3 = severe
Symptom Resolution: Shortness of Breath28 daysThe number of days required to reach a score of 0 from the symptom category of shortness of breath based on a 0-3 scale: 0 = no shortness of breath, 1 = with moderate intensity exercise 2 = with walking on flat surface 3 = short of breath with getting dressed or daily activities
Symptom Resolution: Fatigue28 daysThe number of days required to reach a score of 0 from the symptom category of fatigue based on a 0-3 scale: 1=mild fatigue, 2=moderate fatigue, 3=severe fatigue.
Symptom Resolution: Muscle/body aches28 daysThe number of days required to reach a score of 0 from the symptom category of muscle/body aches based on a 0-3 scale: 1=mild muscle/body aches, 2=moderate muscle/body aches , 3=severe muscle/body aches.
Symptom Resolution: Headache28 daysThe number of days required to reach a score of 0 from the symptom category of headache based on a 0-3 scale: 1=mild headache, 2=moderate headache, 3=severe headache.
Symptom Resolution: New loss of taste28 daysThe number of days required to reach a score of 0 from the symptom category of new loss of taste based on a 0-3 scale: 1=mild loss of taste, 2=moderate loss of taste, 3=severe loss of taste.
Symptom Resolution: New loss of smell28 daysThe number of days required to reach a score of 0 from the symptom category of new loss of smell based on a 0-3 scale: 1=mild loss of smell, 2=moderate loss of smell, 3=severe loss of smell.
Symptom Resolution: Congestion/ runny nose28 daysThe number of days required to reach a score of 0 from the symptom category of congestion/runny nose on a 0-3 scale: 1=mild congestion/runny nose , 2=moderate congestion/runny nose , 3=severe congestion/runny nose .
Symptom Resolution: Fever28 daysThe number of days required to reach a score of 0 from the symptom category of fever based on a 0-3 scale: 0 = ≤98.6, 1 = \>98.6- 100.6, 2 = \> 100.6 - 102.6, 3 = \>102.6
Symptom Resolution: Vomiting28 daysThe number of days required to reach a score of 0 from the symptom category of vomiting on a 0-3 scale: 1=mild vomiting, 2=moderate vomiting, 3=severe vomiting.
Symptom Resolution: Diarrhea28 daysThe number of days required to reach a score of 0 from the symptom category of diarrhea on a 0-3 scale: 1=mild diarrhea, 2=moderate diarrhea, 3=severe diarrhea.
Day 5 Symptoms5 daysTotal symptom composite score at day 5 of study supplementation: Symptom categories of fever based on a 0-3 scale: 0 = ≤98.6, 1 = \>98.6- 100.6, 2 = \> 100.6 - 102.6, 3 = \>102; Cough on a 0-3 scale: 0 = no cough, 1 = mild, 2 = moderate, 3 = severe; Shortness of Breath on a 0-3: 0 = no shortness of breath, 1 = with moderate intensity exercise 2 = with walking on flat surface 3 = short of breath with getting dressed or daily activities; and Fatigue on a 0-3 scale: 0 = No fatigue/energetic, 1=mild fatigue, 2=moderate fatigue, 3=severe fatigue.
Hospitalizations28 daysDifferences in hospitalization events between the study arms
Severity of Symptoms28 daysDifferences in severity of symptoms between study arms
Adjunctive Medications28 daysDifferences in number of patients who were prescribed adjunctive medications for their diagnosis between study arms
Supplementation Side Effects28 daysDifferences in number of patients in study arms who experienced side effects from the supplements.
Symptom Resolution: Nausea28 daysThe number of days required to reach a score of 0 from the symptom category of nausea on a 0-3 scale: 1=mild nausea, 2=moderate nausea, 3=severe nausea.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026