Study to Evaluate the Effect of a Probiotic in COVID-19

  • STATUS
    Recruiting
  • participants needed
    40
  • sponsor
    Bioithas SL
Updated on 19 February 2024
covid-19
SARS
coronavirus infection
acute respiratory syndrome (sars)

Summary

A prospective case-control pilot study to evaluate the possible effect of a probiotic mixture in the improvement of symptoms, the reduction in the number of days of hospitalization and the increase in the percentage of patients with negative PCR after infection with the coronavirus SARS-CoV-2.

Description

In this study, the investigators hypothesize a positive effect of probiotic on the gut microbiome that could led to produce a less severe clinical evolution of the disease.

Details
Condition Coronavirus Infection, Covid 19
Age 18-100 years
Treatment Probiotic
Clinical Study IdentifierNCT04390477
SponsorBioithas SL
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients with a confirmed diagnosis of SARS-Cov.2 infection using the PCR and that require admission to the hospitalization area

Exclusion Criteria

Inability or refusal to sign informed consent
Allergy or intolerance to the intervention product or its components
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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