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A Retrospective Study of COVID-19 Treatments

P

ProgenaBiome

Status

Completed

Conditions

COVID-19 Respiratory Infection
COVID-19 Pneumonia
COVID-19 Acute Respiratory Distress Syndrome
SARS-CoV2 Infection
COVID-19 Lower Respiratory Infection
Covid19
COVID-19 Acute Bronchitis
SARS-CoV-2 Acute Respiratory Disease

Treatments

Other: No Intervention Used

Study type

Observational

Funder types

Other

Identifiers

NCT04949230
PRG-051

Details and patient eligibility

About

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

Full 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.

Enrollment

300 patients

Sex

All

Ages

18+ months old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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:

Trial design

300 participants in 1 patient group

COVID-19 Patients
Description:
Subjects who have recovered from COVID-19
Treatment:
Other: No Intervention Used

Trial contacts and locations

1

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Central trial contact

Ginger Aurella; Jordan E Daniels, MS

Data sourced from clinicaltrials.gov

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