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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04590274
Other study ID # CTP-HCQ-COVID19
Secondary ID
Status Withdrawn
Phase Phase 1
First received
Last updated
Start date November 2020
Est. completion date December 2021

Study information

Verified date December 2021
Source International Brain Research Foundation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Coronavirus Disease 2019 (COVID-19) (previously called 2019-nCOV acute respiratory disease) is caused by SARS-CoV-2, a positive-sense single-stranded RNA virus of the coronavirus family. The coronaviruses are largely responsible for the common cold, the 2002 SARS outbreak in Guangdong, China, the 2012 MERS outbreak in Saudi Arabia, and the present COVID-19 outbreak that originated in Wuhan, China. Much has been reported by way of systemic injury caused by COVID-19 affecting the cardiovascular, hepatic, nervous systems. These conditions are likely the result of the virus overwhelming the immune system. For these reasons, the investigators wish to conduct this study using existing medications off-label, and over-the-counter supplements to support the immune response, prevent lasting injury, and hasten the recovery from COVID-19.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1) Patients must have one or more of the following: 1. confirmed diagnosis of active SARS-CoV-2 infection, diagnosed with PCR 2. continued close contact with an individual with suspected SARS-CoV-2 infection 3. at risk for SARS-CoV-2 infection in the opinion of the treating physician or Principal Investigator. Exclusion Criteria: 1) Patients must not have any uncontrolled disease such as: 1. cardiovascular disease 2. hepatic disease 3. renal disease 4. metabolic disease 5. other diseases or insufficiencies

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Hydroxychloroquine
Hydroxychloroquine
Dietary Supplement:
Vitamins and Minerals
elemental Zinc Vitamin C Vitamin D3 N-acetylcysteine Elderberry Quercetin
Drug:
Azithromycin
Azithromycin

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
International Brain Research Foundation

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of individuals who develop COVID-19 symptoms The investigators will compare what percentage of participants in this study go on to develop COVID-19 symptoms, as compared to individuals not on the medicational regimen in this study. 6 months from study start
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