Evaluation of the effectiveness of probiotics on post-COVID-19 conditions.

  • Funded by Canadian Institutes of Health Research (CIHR)
  • Total publications:251 publications

Grant number: Unknown

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Key facts

  • Disease

    COVID-19
  • start year

    2021
  • Known Financial Commitments (USD)

    $787,845.67
  • Funder

    Canadian Institutes of Health Research (CIHR)
  • Principal Investigator

    N/A

  • Research Location

    Canada
  • Lead Research Institution

    Université de Sherbrooke
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Supportive care, processes of care and management

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Unspecified

  • Broad Policy Alignment

    Pending

  • Age Group

    Adults (18 and older)

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Google translate: The COVID-19 pandemic has affected more than 138 million people and if vaccination brings significant hope, many questions remain (eg impact of virus variants). Studies show that patients could present symptoms up to 6 months after the acute phase (fatigue, anxiety, etc.). The causes of long-lasting COVID (LONG-COV) are poorly understood but may be related to virus persistence or an inadequate immune response. Our group proposes to study the impact of the intestinal microbiota (intestinal flora) on LONG-COV. We know that: 1) people who have a severe form of COVID-19 (elderly, diabetic...) often have an imbalance of the intestinal microbiota, 2) COVID-19 modifies the microbiota (ex: taking antibiotics) and 3) probiotics can improve the balance of the microbiota. We hypothesize that LONG-COV is associated with the consequences of gut microbiota imbalance and that it is possible to reduce the occurrence of LONG-COV using probiotics. As the intestinal microbiota is closely related to the lungs and the brain, the action of probiotics could also reach the other organs affected by LONG-COV. We are proposing a study that compares the intake of probiotics to that of a placebo. We will include 618 men and women aged 18 and over, symptomatic of COVID-19 with a COVID+ test for 10 days or less. Hospitalized patients (population at risk of LONG-COV) can be included if they returned home within 10 days of diagnosis. The signs of LONG-COV will be studied on the 30th and 90th day (internet or telephone). A group of volunteer patients will take samples (saliva and stool) for virus and microbiota analyses. If successful, probiotics could be used very quickly across Canada (few side effects, affordable costs).]

Publicationslinked via Europe PMC

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Revisiting Spirituality in Physical Therapy Practice: Perceptions of US Practitioners.

Aflibercept for Wet Age-Related Macular Degeneration: A Prospective, Randomized Trial Comparing Treat-And-Extend and Fixed Bimonthly Dosing.

The Concentration and Duration of Lipopolysaccharide Stimulation Produce Different Cytokine Responses in an Ex Vivo Whole Blood Model in Horses.

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