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Randomized Proof-of-Concept Trial to Evaluate the Safety and Explore the Effectiveness of Resveratrol, a Plant Polyphenol, for COVID-19

Primary Purpose

COVID-19

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Resveratrol
Vitamin D3
Sponsored by
Marvin McCreary, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 focused on measuring Coronavirus, SARS-CoV-2, COVID, Vitamin D3, Cholecalciferol, Supplement, Polyphenol, Resveratrol, Stilbene, phytoalexin

Eligibility Criteria

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

Inclusion Criteria:

  • Outpatients who test positive for infection with SARS-CoV-2.
  • Age ≥45 years
  • Mild COVID-19 based on World Health Organization (WHO) Baseline Severity Categorization
  • Symptom duration ≤ 10 days, or <72 hours of new respiratory symptoms.
  • Patient must have access to the internet or a smartphone to complete surveys.
  • English-speaking patients

Exclusion Criteria:

  • Diagnosed or suspected cognitive impairment that would prevent the patient from cooperating with study procedures, as judged by the screening clinician
  • Asymptomatic patients (e.g. patients who were screened without symptoms but tested positive)
  • Known or suspected liver disease or Hepatitis C
  • Known kidney disease with estimate Glomerular Filtration Rate (eGFR) <60
  • Patients on warfarin, Novel Oral Anticoagulants (NOACs), HIV Protease Inhibitors, immunosuppressants, hydroxychloroquine/chloroquine, and other medication with a narrow therapeutic window.
  • Allergy to grapes or rice.
  • Co-morbidities with a high likelihood of hospitalization within 30 days (e.g., current cancer treatment, severe Chronic Obstructive Pulmonary Disease (COPD) or Congestive Heart Failure (CHF))
  • Currently pregnant
  • Hospitalization

Sites / Locations

  • Mt Carmel HealthSystems

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Resveratrol with Vitamin D3

Placebo with Vitamin D3

Arm Description

Resveratrol 1000mg four times per day for 15 days. Vitamin D3 100,000 IU on day 1

Placebo capsules 4 times per day for 15 days. Vitamin D3 100,000 IU on day 1

Outcomes

Primary Outcome Measures

Hospitalization Rates for COVID-19
Number of study participants admitted to the hospital within 21 days of randomization

Secondary Outcome Measures

ICU Admission Rates
Number of study participants admitted within 21 who subsequently get admitted to the ICU
Invasive Ventilation Rates
Number of study participants who get admitted with 21 day of randomization who receiving invasive ventilation.
Pneumonia
Number of study participants are diagnosed with pneumonia with 21 day of randomization
Pulmonary Embolism
Number of study participants are diagnosed with pulmonary embolism with 21 day of randomization
Death
Number of study participants who died with 21 day of randomization

Full Information

First Posted
May 22, 2020
Last Updated
February 22, 2023
Sponsor
Marvin McCreary, MD
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1. Study Identification

Unique Protocol Identification Number
NCT04400890
Brief Title
Randomized Proof-of-Concept Trial to Evaluate the Safety and Explore the Effectiveness of Resveratrol, a Plant Polyphenol, for COVID-19
Official Title
Randomized Double-Blind Placebo-Controlled Proof-of-Concept Trial of Resveratrol, a Plant Polyphenol, for the Outpatient Treatment of Mild Coronavirus Disease (COVID-19)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Terminated
Why Stopped
Feasibility
Study Start Date
September 13, 2020 (Actual)
Primary Completion Date
March 1, 2021 (Actual)
Study Completion Date
March 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Marvin McCreary, MD

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Resveratrol is a plant polyphenol (that is sold commercially as a supplement) that might help fight coronavirus as well as help protect the body from the effects of disease (COVID-19) caused by the infection. In this proof-of-concept pilot study we will compare the effects of resveratrol to placebo to assess the safety of the resveratrol and explore effectiveness.
Detailed Description
This randomized placebo-controlled trial is for the outpatient treatment of (Coronavirus Disease 2019) COVID-19. The purpose of this trial is to evaluate the safety and explore the effectiveness of resveratrol, a plant polyphenol, being re-purposed for patients with early COVID-19. Published in vitro data supports that this polyphenol inhibits coronavirus replication while separately published in silico (computer molecular docking analysis) reports have identified specific molecular targets of resveratrol against (Severe Acute Respiratory Syndrome - Coronavirus 2) SARS-CoV-2. Animal studies also demonstrate that resveratrol is effective at preventing lung injury and death in certain animal models of viral infections. Furthermore, the products long history as an anti-inflammatory might prevent the cytokine storm that is associated with worse outcomes in COVID-19. 200 subjects, 45 and older, (100 receiving the plant polyphenol, 100 receiving placebo) will be enrolled in study to compare whether taking resveratrol will reduce the rate of hospitalization. Subjects will take capsules 4 times a day for a minimum of 7 days (up to 15 days depending on duration of symptoms) plus both groups will receive Vitamin D3 100,000 IU to augment the effects of resveratrol. Resveratrol will be given as 1gm 4 times per day. Placebo tablets will contain brown rice flour in visually identical capsules. The primary outcome measure for this trial is reduction in hospitalization at 21 days from enrollment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19
Keywords
Coronavirus, SARS-CoV-2, COVID, Vitamin D3, Cholecalciferol, Supplement, Polyphenol, Resveratrol, Stilbene, phytoalexin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
105 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Resveratrol with Vitamin D3
Arm Type
Active Comparator
Arm Description
Resveratrol 1000mg four times per day for 15 days. Vitamin D3 100,000 IU on day 1
Arm Title
Placebo with Vitamin D3
Arm Type
Placebo Comparator
Arm Description
Placebo capsules 4 times per day for 15 days. Vitamin D3 100,000 IU on day 1
Intervention Type
Drug
Intervention Name(s)
Resveratrol
Other Intervention Name(s)
Placebo
Intervention Description
Resveratrol vs placebo given for 15 days.
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3
Intervention Description
Vitamin D3 100,000 IU given on day one.
Primary Outcome Measure Information:
Title
Hospitalization Rates for COVID-19
Description
Number of study participants admitted to the hospital within 21 days of randomization
Time Frame
21 days from study randomization
Secondary Outcome Measure Information:
Title
ICU Admission Rates
Description
Number of study participants admitted within 21 who subsequently get admitted to the ICU
Time Frame
21 days from randomization
Title
Invasive Ventilation Rates
Description
Number of study participants who get admitted with 21 day of randomization who receiving invasive ventilation.
Time Frame
21 days from randomization
Title
Pneumonia
Description
Number of study participants are diagnosed with pneumonia with 21 day of randomization
Time Frame
21 days from randomization
Title
Pulmonary Embolism
Description
Number of study participants are diagnosed with pulmonary embolism with 21 day of randomization
Time Frame
21 days from start of randomization.
Title
Death
Description
Number of study participants who died with 21 day of randomization
Time Frame
Within 21 days from randomization
Other Pre-specified Outcome Measures:
Title
Adverse Events
Description
Diarrhea, nausea, abdominal cramping
Time Frame
60 days from randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Outpatients who test positive for infection with SARS-CoV-2. Age ≥45 years Mild COVID-19 based on World Health Organization (WHO) Baseline Severity Categorization Symptom duration ≤ 10 days, or <72 hours of new respiratory symptoms. Patient must have access to the internet or a smartphone to complete surveys. English-speaking patients Exclusion Criteria: Diagnosed or suspected cognitive impairment that would prevent the patient from cooperating with study procedures, as judged by the screening clinician Asymptomatic patients (e.g. patients who were screened without symptoms but tested positive) Known or suspected liver disease or Hepatitis C Known kidney disease with estimate Glomerular Filtration Rate (eGFR) <60 Patients on warfarin, Novel Oral Anticoagulants (NOACs), HIV Protease Inhibitors, immunosuppressants, hydroxychloroquine/chloroquine, and other medication with a narrow therapeutic window. Allergy to grapes or rice. Co-morbidities with a high likelihood of hospitalization within 30 days (e.g., current cancer treatment, severe Chronic Obstructive Pulmonary Disease (COPD) or Congestive Heart Failure (CHF)) Currently pregnant Hospitalization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marvin R McCreary
Organizational Affiliation
Mount Carmel Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mt Carmel HealthSystems
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43213
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
35768453
Citation
McCreary MR, Schnell PM, Rhoda DA. Randomized double-blind placebo-controlled proof-of-concept trial of resveratrol for outpatient treatment of mild coronavirus disease (COVID-19). Sci Rep. 2022 Jun 29;12(1):10978. doi: 10.1038/s41598-022-13920-9.
Results Reference
derived
PubMed Identifier
34545357
Citation
McCreary MR, Schnell PM, Rhoda DA. Randomized Double-blind Placebo-controlled Proof-of-concept Trial of Resveratrol for Outpatient Treatment of Mild Coronavirus Disease (COVID-19). Res Sq. 2021 Sep 13:rs.3.rs-861831. doi: 10.21203/rs.3.rs-861831/v1. Preprint.
Results Reference
derived
Links:
URL
https://www.nature.com/articles/s41598-022-13920-9
Description
Peer reviewed final publication

Learn more about this trial

Randomized Proof-of-Concept Trial to Evaluate the Safety and Explore the Effectiveness of Resveratrol, a Plant Polyphenol, for COVID-19

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