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Evaluation of the Probiotic Lactobacillus Coryniformis K8 on COVID-19 Prevention in Healthcare Workers

B

Biosearch Life

Status

Unknown

Conditions

Covid-19

Treatments

Dietary Supplement: Control
Dietary Supplement: Probiotic

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

The aim of the present study is to evaluate the effects of Lactobacillus coryniformis K8 consumption on the incidence and severity of Covid-19 in health workers exposed to the virus. This is a preventive study

Enrollment

314 estimated patients

Sex

All

Ages

20+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Persons over 20 years of age.
  2. Active healthcare personnel, who attend patients with COVID-19 disease, including all professional categories, medicine, nursing and warders.
  3. Ability to complete surveys.
  4. Signature of informed consent

Exclusion criteria

  1. Person with positive test of COVID-19 confirmed by PCR test or serology
  2. Person with concomitant pathology HIV, transplant, active oncology or other type of active immunosuppression
  3. Pregnant women or women with intention to become pregnant in the next 2 months.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

314 participants in 2 patient groups, including a placebo group

Probiotic
Experimental group
Description:
Experimental group who will receive one capsule of Lactobacillus K8 per day (3x10\^9 cfu/day).
Treatment:
Dietary Supplement: Probiotic
Control
Placebo Comparator group
Description:
Control group who will receive a daily placebo capsule consisting of maltodextrin
Treatment:
Dietary Supplement: Control

Trial contacts and locations

1

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Central trial contact

Raquel Rodriguez Blanque

Data sourced from clinicaltrials.gov

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