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Probiotic
Probiotics for Long COVID Symptoms
N/A
Recruiting
Led By Michael E Widlansky, MD, MPH
Research Sponsored by Medical College of Wisconsin
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Ages 18 to 89 years
Be older than 18 years old
Must not have
Subjects currently taking Vitamin K antagonists such as coumadin or warfarin
History of cognitive impairment/inability to follow study procedures
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 weeks
Summary
This trial tests whether taking a probiotic called Lp299v can help people who have long-term symptoms after COVID-19. The probiotic aims to reduce inflammation and improve blood vessel function. Adults aged 18-89 with these symptoms will take the supplement for a period of time to see if it helps. Probiotics have shown benefits in a variety of diseases, including respiratory infections, and may be beneficial in the adjunctive treatment of COVID-19.
Who is the study for?
This trial is for adults aged 18-89 who have had COVID-19 and are experiencing lingering symptoms known as PASC. They must be within 30 to 180 days post-diagnosis. People with daily alcohol use, recent antibiotics, blood thinner usage like warfarin, pregnancy, cognitive issues preventing study compliance, unstable heart disease or certain chronic conditions can't participate.
What is being tested?
The trial tests if a probiotic called Lactobacillus plantarum (Lp299v) in capsule form can improve blood vessel function in those with PASC by reducing inflammation and immune system activation compared to a placebo made of potato starch capsules.
What are the potential side effects?
While the specific side effects aren't listed here, probiotics like Lp299v typically may cause digestive discomfort such as gas or bloating. Placebos generally have no active ingredients but can sometimes cause mild reactions due to psychological factors.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 18 and 89 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently taking blood thinners like coumadin or warfarin.
Select...
I have no history of cognitive issues affecting my ability to follow study instructions.
Select...
I have short gut syndrome, inflammatory bowel disease, or an ileostomy.
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I haven't had chronic kidney, liver diseases, or cancer treatments in the last 3 years.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 8 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Brachial Artery Flow Mediated Dilation (FMD%)
Secondary study objectives
Brachial Artery Resting Diameter
Carotid-Femoral Pulse Wave Velocity (cfPWV)
Cell-Free Mitochondrial DNA (cf-mtDNA)
+7 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Lp299vExperimental Treatment1 Intervention
Subjects will consume 20 billion colony forming units of Lp299v (2 capsules) once daily for 8 weeks.
Group II: Heat-killed placebo controlPlacebo Group1 Intervention
Subjects will consume potato starch (2 capsules) once daily for 8 weeks.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for COVID-19 often target viral replication, inflammation, and immune modulation. For example, Lactobacillus plantarum 299v, a probiotic, reduces circulating cell-free mitochondrial DNA (cf-mtDNA), decreases toll-like receptor 9 (TLR9) activation, and lowers inflammation.
These actions are crucial because they help mitigate the excessive inflammatory response and endothelial dysfunction associated with COVID-19, potentially improving patient outcomes and reducing complications.
A naturopathic treatment approach for mild and moderate COVID-19: A retrospective chart review.The effect of probiotics on respiratory tract infection with special emphasis on COVID-19: Systemic review 2010-20.Effects of Probiotics in Conditions or Infections Similar to COVID-19 on Health Outcomes: An Evidence Analysis Center Scoping Review.
A naturopathic treatment approach for mild and moderate COVID-19: A retrospective chart review.The effect of probiotics on respiratory tract infection with special emphasis on COVID-19: Systemic review 2010-20.Effects of Probiotics in Conditions or Infections Similar to COVID-19 on Health Outcomes: An Evidence Analysis Center Scoping Review.
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Who is running the clinical trial?
Medical College of WisconsinLead Sponsor
628 Previous Clinical Trials
1,179,796 Total Patients Enrolled
Michael E Widlansky, MD, MPHPrincipal InvestigatorMedical College of Wisconsin
2 Previous Clinical Trials
43 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You drink alcohol every day, which could affect the way the study drug works.I was diagnosed with COVID-19 between 30 to 180 days ago.I am currently taking blood thinners like coumadin or warfarin.I have no history of cognitive issues affecting my ability to follow study instructions.I have not taken antibiotics in the last four weeks.I am between 18 and 89 years old.I have not had new heart symptoms or events in the last 30 days.I have been diagnosed with long COVID by a doctor.I have short gut syndrome, inflammatory bowel disease, or an ileostomy.I haven't had chronic kidney, liver diseases, or cancer treatments in the last 3 years.
Awards:
This trial has 0 awards, including:Research Study Groups:
This trial has the following groups:- Group 1: Lp299v
- Group 2: Heat-killed placebo control
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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