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Synbiotic Therapy of Gastrointestinal Symptoms During Covid-19 Infection (SynCov)

Primary Purpose

COVID

Status
Active
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Omnibiotic AAD
Placebo
Sponsored by
Medical University of Graz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria

  • 18 years or older
  • Covid-19 infection diagnosed by a positive SARS-Cov-2 PCR (Polymerase chain reaction) result from a nasopharyngeal swab
  • Informed (tele)consent Exclusion criteria
  • Pre-existing diarrhoea (including but not restricted to chronic inflammatory bowel disease, chronic diarrhea of other causes, acute diarrheal illness -4 to -1 week before inclusion)
  • Antibiotic therapy -4 to -1 week before inclusion
  • Probiotic treatment -4 to -1 week before inclusion
  • Technical difficulties to perform telemedicine study visits

Sites / Locations

  • Department of Internal Medicine, Medical University of Graz

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Probiotic

Placebo

Arm Description

Group 1: receiving a probiotic mixture (Omni-Biotic® 10 AAD) twice a day

Group 2: receiving a similar looking and tasting placebo without bacteria twice a day

Outcomes

Primary Outcome Measures

Stool calprotectin
measured by ELISA

Secondary Outcome Measures

Stool frequency
stool evacuations per days
Stool consistency
Stool consistency according to Bristol stool scale for each evacuation, score 1-7, a higher score means a lower stool consistancy
Gastrointestinal symptoms
presence of anorexia, nausea, vomiting, abdominal pain, bloating (yes/no)
Duration of Covid-19 disease
days patients feel sick, are not able to work or are on sick leave
Severity of Covid-19 disease
mild/moderate/severe
Diarrhea
3 or more stool evacuations, consistency Bristol stool scale 5-7
Stool Zonulin
measured by ELISA
Microbiome composition
16S RNA sequencing

Full Information

First Posted
June 4, 2020
Last Updated
January 23, 2023
Sponsor
Medical University of Graz
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1. Study Identification

Unique Protocol Identification Number
NCT04420676
Brief Title
Synbiotic Therapy of Gastrointestinal Symptoms During Covid-19 Infection
Acronym
SynCov
Official Title
Synbiotic Therapy of Gastrointestinal Symptoms During Covid-19 Infection: A Randomized, Double-blind, Placebo Controlled, Telemedicine Study (SynCov Study)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 24, 2020 (Actual)
Primary Completion Date
December 1, 2021 (Actual)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Graz

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
We hypothesize that the intake of Omni-Biotic® 10 AAD can reduce intestinal inflammation and improves dysbiosis in Covid-19 disease. We further hypothesize that Omni-Biotic® 10 AAD can reduce the duration of diarrhea, stool frequency, improve stool consistency, improve other gastrointestinal symptoms of Covid-19, reduce disease duration and severity. The investigators aim to perform a randomized, double blind, placebo-controlled study using telemedicine in patients with Covid-19 disease.
Detailed Description
The outbreak of the novel coronavirus (SARS-CoV-2)-infected disease (COVID-19) began in Wuhan, Hubei province in December 2019, spread throughout China in early 2020 and developed as a pandemic thereafter. Although the virus mainly causes respiratory symptoms, GI (gastrointestinal) presentations have been reported in and outside of China. Patients may present with anorexia, nausea, vomiting, diarrhea and abdominal discomfort. Also, faecal-oral transmission of the virus is currently discussed. Preliminary, unpublished data from China suggest that patients with GI symptoms may suffer more frequently from severe courses of the disease. Clinical studies show an incidence rate of diarrhea ranging from 2% to 50% of cases. It may precede or trail respiratory symptoms. A pooled analysis revealed an overall percentage of diarrhea onset of 10.4%. SARS-CoV-2 uses the angiotensin-converting enzyme 2 (ACE2) for cellular entry. ACE2 is expressed in the small intestinal epithelia as well as in the upper esophagus, liver, and colon. SARS-CoV-2 binding affinity to ACE2 is significantly higher (10-20 times) compared with SARS-CoV. Diarrhea is associated with prolonged symptoms and viral carriage. Clinical information on the characteristics of Covid-19 diarrhea is scarce. The duration of diarrhea is around 4 days with 3-4 loose stools per day. Faecal calprotectin is elevated in stool of patients with Covid-19 diarrhea, indicating a relation between gastrointestinal symptoms and this well-established inflammation biomarker. So far, no therapy is available for Covid-19 infection in general or for Covid-19 induced diarrhea. Rehydration and potassium monitoring should be performed as in all patients with diarrhea. It is important to underline that antivirals and antibiotics are often used for COVID-19 treatment or treatment of bacterial superinfections, involving a likely alteration of the gut microbiota and causing diarrhea. It is therefore plausible that the gut microbiota could be a new therapeutic target and that probiotics or synbiotics (combination of probiotics with prebiotics) could have a role in the management of these patients. The China's National Health Commission recommended the use of probiotics for the treatment of patients with severe COVID-19 in order to preserve intestinal balance and to prevent secondary bacterial infections without any available clinical studies to support this and probiotics apparently were used in Zhejiang during the Covid-19 pandemic. Although there is no specific data on the effects of probiotics on SARS-CoV2 infections, meta-analyses show that probiotics are effective in the treatment of upper respiratory tract infections and viral gastroenteritis of other origins. Furthermore, Enterococcus faecium has been shown to have antiviral effects in enteropathogenic coronavirus transmissible gastroenteritis virus infections in piglets. We therefore aim to assess the role of synbiotics in the therapy of Covid-19 infection with gastrointestinal symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Probiotic
Arm Type
Active Comparator
Arm Description
Group 1: receiving a probiotic mixture (Omni-Biotic® 10 AAD) twice a day
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Group 2: receiving a similar looking and tasting placebo without bacteria twice a day
Intervention Type
Dietary Supplement
Intervention Name(s)
Omnibiotic AAD
Other Intervention Name(s)
Ecologic AAD
Intervention Description
Bacterial strains in Omni-Biotic® 10 AAD are Bifidobacterium bifidum W23, Bifidobacterium lactis W51, Enterococcus faecium W54, Lactobacillus acidophilus W37, Lactobacillus acidophilus W55, Lactobacillus paracasei W20, Lactobacillus plantarum W1, Lactobacillus plantarum W62, Lactobacillus rhamnosus W71 and Lactobacillus salivarius W24 which are embedded in a matrix containing maize starch, maltodextrin, inulin, potassium chloride, hydrolysed rice protein, magnesium sulphate, fructooligosaccharide (FOS), enzymes (amylases), vanilla flavour and manganese sulphate
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
matrix containing maize starch, maltodextrin, inulin, potassium chloride, hydrolysed rice protein, magnesium sulphate, fructooligosaccharide (FOS), enzymes (amylases), vanilla flavour and manganese sulphate.
Primary Outcome Measure Information:
Title
Stool calprotectin
Description
measured by ELISA
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Stool frequency
Description
stool evacuations per days
Time Frame
30 days
Title
Stool consistency
Description
Stool consistency according to Bristol stool scale for each evacuation, score 1-7, a higher score means a lower stool consistancy
Time Frame
30 days
Title
Gastrointestinal symptoms
Description
presence of anorexia, nausea, vomiting, abdominal pain, bloating (yes/no)
Time Frame
30 days
Title
Duration of Covid-19 disease
Description
days patients feel sick, are not able to work or are on sick leave
Time Frame
30 days
Title
Severity of Covid-19 disease
Description
mild/moderate/severe
Time Frame
30 days
Title
Diarrhea
Description
3 or more stool evacuations, consistency Bristol stool scale 5-7
Time Frame
30 days
Title
Stool Zonulin
Description
measured by ELISA
Time Frame
30 days
Title
Microbiome composition
Description
16S RNA sequencing
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria 18 years or older Covid-19 infection diagnosed by a positive SARS-Cov-2 PCR (Polymerase chain reaction) result from a nasopharyngeal swab Informed (tele)consent Exclusion criteria Pre-existing diarrhoea (including but not restricted to chronic inflammatory bowel disease, chronic diarrhea of other causes, acute diarrheal illness -4 to -1 week before inclusion) Antibiotic therapy -4 to -1 week before inclusion Probiotic treatment -4 to -1 week before inclusion Technical difficulties to perform telemedicine study visits
Facility Information:
Facility Name
Department of Internal Medicine, Medical University of Graz
City
Graz
ZIP/Postal Code
8010
Country
Austria

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Upload of microbiome sequences and metadata to a repository
IPD Sharing Time Frame
1 year after completion
IPD Sharing Access Criteria
free

Learn more about this trial

Synbiotic Therapy of Gastrointestinal Symptoms During Covid-19 Infection

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