Evaluation of a Synbiotic Formula in Patient With COVID-19
Primary Purpose
Coronavirus
Status
Unknown status
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Health supplements
Sponsored by
About this trial
This is an interventional other trial for Coronavirus focused on measuring microbiota
Eligibility Criteria
Inclusion Criteria:
- Aged 18 or above; and
- A confirmed diagnosis of SARS-Cov.2 infection using the PCR according to the standard of according to Centre for Health Protection, Department of Health, HK and released from isolation at recruitment.
- Written informed consent obtained
Exclusion Criteria:
- Known allergy or intolerance to the intervention product or its components
- Any known medical condition that would prevent taking oral probiotics or increase risks associated with probiotics including but not limited to inability to swallow/aspiration risk and no other methods of delivery (e.g., no G/J tube)
Known increased infection risk due to immunosuppression such as:
- Prior organ or hematopoietic stem cell transplant
- Neutropenia (ANC <500 cells/ul)
- HIV and CD4 <200 cells/ul
Known increased infection risk due to endovascular due to:
- Rheumatic heart disease
- Congenital heart defect,
- Mechanical heart valves
- Endocarditis
- Endovascular grafts
- Permanent endovascular devices such as permanent (not short-term) hemodialysis catheters, pacemakers, or defibrillators
- Documented pregnancy
Sites / Locations
- Chinese University of Hong KongRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Health supplements
Arm Description
One arm only
Outcomes
Primary Outcome Measures
Changes in gut microbiome
Changes in the gut microbiome (bacteria, virome and fungome) measured by metagenomics at week 5 compared to baseline
Secondary Outcome Measures
Changes in fecal bacteria metabolites
Changes in fecal bacteria metabolites by PCR at different time points
Change in plasma cytokines including IL-6, IL-IB, TNF-a and CXCL-10
Change in plasma cytokines level at week 5 compared with baseline
Trend in symptom score
Trend of symptom score at different time points, ranges from 26-104. The higher the score, the worse the symptoms.
Change in Quality of life measured by EQ-5D-5L
Change in score on Quality of life using EQ-5D-5L at different time points. EQ-5D-5L is a self-assessed, health related, quality of life questionnaire. The scale measures quality of life on a 5-component scale including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The index can be calculated by deducting the appropriate weights from 1, the value for full health (i.e. state 11111). Each category ranges from 1 to 5. The small the number, the better the health. The EQ-VAS is a vertical visual analogue scale that ranges 0-100 (higher score indicates better imaginable health).
Change in Quality of life measured by SF-12
Change in score on Quality of life using SF-12 at different time points. SF-12 is a self-reported outcome measure assessing the impact of health on an individual's everyday life. There are formulas for transformation of scale scores so that they will range from 0-100. High score in functioning items indicates better functioning while high score in pain items indicates freedom from pain.
Duration of gastrointestinal symptoms
Duration of gastrointestinal symptoms such as anorexia, nausea, vomiting, abdominal pain, bloating within 4 weeks.
Adverse event assessment
Number of adverse event
Full Information
NCT ID
NCT04730284
First Posted
August 25, 2020
Last Updated
January 28, 2021
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT04730284
Brief Title
Evaluation of a Synbiotic Formula in Patient With COVID-19
Official Title
Evaluation of a Synbiotic Formula in Patient With COVID-19
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 25, 2020 (Actual)
Primary Completion Date
September 30, 2021 (Anticipated)
Study Completion Date
March 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
A series of microbiota were correlated inversely with the disease severity and virus load. Gut microbiota could play a role in modulating host immune response and potentially influence disease severity and outcomes.
Detailed Description
Coronavirus can target multiple organs due to the hyperactive immune response with cytokine storms. Several studies have detected SARS-CoV-2 in stool samples and indicated that the virus could spread via faeces. Importantly, COVID-19 uses the same receptor as SARS and this doorway can also be found in the intestine. The cell entry receptor, known as angiotensin converting enzyme 2 (ACE2) receptor mediate entry of SARS-CoV-2 and is highly expressed in small bowel enterocytes. ACE2 is important in controlling intestinal inflammation and its disruption may lead to diarrhoea. In our previous study, stool samples from 15 patients with COVID-19 were analysed. Depleted symbionts and gut dysbiosis were noted even after patients were detected negative of SARS-CoV-2. A series of microbiota were correlated inversely with the disease severity and virus load. Gut microbiota could play a role in modulating host immune response and potentially influence disease severity and outcomes.
In July 2020, there are more than 15 billion confirmed cases globally with 620 thousand deaths. Currently, there are more than 2000 confirmed cases of COVID-19 in Hong Kong. It is important to rebalance the gut microbiota in COVID-19 patients and to improve the symptoms and the quality of life of these patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronavirus
Keywords
microbiota
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Health supplements
Arm Type
Experimental
Arm Description
One arm only
Intervention Type
Other
Intervention Name(s)
Health supplements
Intervention Description
tailor-made Synbiotics, 4g per day for 28 days
Primary Outcome Measure Information:
Title
Changes in gut microbiome
Description
Changes in the gut microbiome (bacteria, virome and fungome) measured by metagenomics at week 5 compared to baseline
Time Frame
week 5
Secondary Outcome Measure Information:
Title
Changes in fecal bacteria metabolites
Description
Changes in fecal bacteria metabolites by PCR at different time points
Time Frame
weeks 2, 4, 5, 8 and months 3, 6, 9 and 12
Title
Change in plasma cytokines including IL-6, IL-IB, TNF-a and CXCL-10
Description
Change in plasma cytokines level at week 5 compared with baseline
Time Frame
week 5
Title
Trend in symptom score
Description
Trend of symptom score at different time points, ranges from 26-104. The higher the score, the worse the symptoms.
Time Frame
weeks 2, 4, 5, 8 and months 3, 6, 9 and 12
Title
Change in Quality of life measured by EQ-5D-5L
Description
Change in score on Quality of life using EQ-5D-5L at different time points. EQ-5D-5L is a self-assessed, health related, quality of life questionnaire. The scale measures quality of life on a 5-component scale including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The index can be calculated by deducting the appropriate weights from 1, the value for full health (i.e. state 11111). Each category ranges from 1 to 5. The small the number, the better the health. The EQ-VAS is a vertical visual analogue scale that ranges 0-100 (higher score indicates better imaginable health).
Time Frame
weeks 2, 4, 5, 8 and months 3, 6, 9 and 12
Title
Change in Quality of life measured by SF-12
Description
Change in score on Quality of life using SF-12 at different time points. SF-12 is a self-reported outcome measure assessing the impact of health on an individual's everyday life. There are formulas for transformation of scale scores so that they will range from 0-100. High score in functioning items indicates better functioning while high score in pain items indicates freedom from pain.
Time Frame
weeks 2, 4, 5, 8 and months 3, 6, 9 and 12
Title
Duration of gastrointestinal symptoms
Description
Duration of gastrointestinal symptoms such as anorexia, nausea, vomiting, abdominal pain, bloating within 4 weeks.
Time Frame
4 weeks
Title
Adverse event assessment
Description
Number of adverse event
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged 18 or above; and
A confirmed diagnosis of SARS-Cov.2 infection using the PCR according to the standard of according to Centre for Health Protection, Department of Health, HK and released from isolation at recruitment.
Written informed consent obtained
Exclusion Criteria:
Known allergy or intolerance to the intervention product or its components
Any known medical condition that would prevent taking oral probiotics or increase risks associated with probiotics including but not limited to inability to swallow/aspiration risk and no other methods of delivery (e.g., no G/J tube)
Known increased infection risk due to immunosuppression such as:
Prior organ or hematopoietic stem cell transplant
Neutropenia (ANC <500 cells/ul)
HIV and CD4 <200 cells/ul
Known increased infection risk due to endovascular due to:
Rheumatic heart disease
Congenital heart defect,
Mechanical heart valves
Endocarditis
Endovascular grafts
Permanent endovascular devices such as permanent (not short-term) hemodialysis catheters, pacemakers, or defibrillators
Documented pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kristy Ho, Bsc
Phone
85235053855
Email
hiutungho@cuhk.edu.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Kitty Cheung, MPH
Phone
85226373225
Email
kittyccy@cuhk.edu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Siew Ng, PhD
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chinese University of Hong Kong
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
12. IPD Sharing Statement
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Evaluation of a Synbiotic Formula in Patient With COVID-19
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