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NCT04949230 Clinical Trial

A Retrospective Study of COVID-19 Treatments

Covid19 Clinical Trial

Official title:
A Retrospective Study to Analyze Efficacy of COVID-19 Treatments

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04949230
Other study ID # PRG-051
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 19, 2021
Est. completion date February 15, 2024

Study information
Verified date February 2024
Source ProgenaBiome
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Surveys administered to subjects who have recovered from COVID-19 to assess how effective their treatment was.

Description:

Subjects who have recovered from COVID-19 will answer questions regarding the severity of their illness, symptoms experienced, what treatment they received, and how long they were ill.

Recruitment information / eligibility
Status Completed
Enrollment 300
Est. completion date February 15, 2024
Est. primary completion date February 15, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Months and older
Eligibility Inclusion Criteria: 1. Signed informed consent, demonstrating that the patient understands the procedures required for the study and the purpose of the study 2. Male or female of 18 years of age or older 3. Diagnosis of COVID-19 infection by RT- PCR 4. Recovery from COVID-19 Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• No Intervention Used
There is no intervention in this study

Locations
Country Name City State
United States Ginger Aurella Ventura California

Sponsors (1)
Lead Sponsor Collaborator
ProgenaBiome

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Survey Response Answers given by subjects on their recovery from COVID-19 One hour
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