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An Evaluation of a Synbiotic Formula for Patients With COVID-19 Infection

Primary Purpose

Covid19, Microbiota

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Health supplements
Sponsored by
Siew Chien NG
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Covid19

Eligibility Criteria

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

Inclusion Criteria:

  1. Aged 18 or above; and
  2. 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 at recruitment and that require admission to the hospitalization area; and
  3. Written informed consent is obtained

Exclusion Criteria:

  1. Subjects admitted to Intensive Care Unit or on ventilator
  2. Known allergy or intolerance to the intervention product or its components
  3. 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)
  4. 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
  5. Known history or active endocarditis
  6. Recent on CAPD or hemodialysis-
  7. Documented pregnancy

Sites / Locations

  • The Chinese University of Hong Kong

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Health supplements + standard care

Standard care

Arm Description

28 days of health supplements (Synbiotic) daily plus standard care

No intervention

Outcomes

Primary Outcome Measures

Combined symptom score
Combined symptom score improvement of the first 4 weeks. Symptoms score assessment ranges from 20-80. The higher the score, the worse the symptoms.

Secondary Outcome Measures

Clinical improvement
Compare the number and severity of symptoms existing by checking the list in symptoms assessment such as cough, shortness of breath, fever and gastrointestinal symptoms like anorexia, nausea, vomiting, abdominal pain, bloating before and during the study
Time to develop antibody against SARS-CoV-2
Compare the time to develop antibody against SARS-CoV-2 in both group
Quality of life measured by EQ-5D-5L
Improvement of quality of life measured by EQ-5D-5L. 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).
Quality of life measured by SF-12
Improvement of quality of life measured by SF-12. 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 hospital stay
Measure the duration of hospital stay in both group
Time to negative PCR
Compare the time to negative PCR in both group
Trend of symptom score
Trend of symptom score, ranges from 26-104. The higher the score, the worse the symptoms.
Gastrointestinal symptoms
Duration of gastrointestinal symptoms such as anorexia, nausea, vomiting, abdominal pain, bloating within 4 week.
Changes in fecal bacteria metabolites
Changes in fecal bacteria metabolites measured by PCR at different time points
Change in plasma cytokines level
Change in plasma cytokines level at week 2 and week 5 compared with baseline
Changes in the gut microbiome
Changes in the gut microbiome (bacteria, virome and fungome) measured by metagenomics at different time points (weeks 1, 2, 3, 4, 5 and months 3, 6, 9 and 12) compared to baseline
Number of admission to Intensive Care Unit
Number of admission to Intensive Care Unit
Number of subjects with home discharge
Number of subjects with home discharge
Number of mortality
Number of mortality
Number of days absent from work
Number of days absent from work since admission
Change of quality of life questionnaire
Change in score on Quality of life using EQ-5D-5L and SF-12. 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). While the 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.
Number of adverse event
Number of adverse event

Full Information

First Posted
August 11, 2020
Last Updated
November 1, 2022
Sponsor
Siew Chien NG
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1. Study Identification

Unique Protocol Identification Number
NCT04581018
Brief Title
An Evaluation of a Synbiotic Formula for Patients With COVID-19 Infection
Official Title
An Evaluation of a Synbiotic Formula for Symptom Improvement in Hospitalised Patients With COVID-19 Infection
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
August 13, 2020 (Actual)
Primary Completion Date
December 31, 2021 (Actual)
Study Completion Date
July 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Siew Chien NG

4. Oversight

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

5. Study Description

Brief Summary
In December 2019, a cluster of pneumonia cases of unidentified cause emerged in Wuhan,was identified as the culprit of this disease currently being identified as "Coronavirus Disease 2019" (COVID-19) by World Health Organization. Coronavirus was found to not only target the patient's lungs but also multiple organs. Around 2-33% of Coronavirus Disease-19 patients developed gastrointestinal symptoms. Studies have shown that Severe acute respiratory syndrome coronavirus 2 (SAR-CoV-2) was found in patient's feces, suggesting that the virus can spread through feces. 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. The investigators are uncertain about the impact of synbiotic on patients with COVID-19. However, a therapeutic strategy aiming at investigating the gut Imicrobiota of patients with COVID-9 who take synbiotic or not, leading to lesser progression to severe disease, less hospital stay and improved quality of life.
Detailed Description
In December 2019, a cluster of pneumonia cases of unidentified cause emerged in Wuhan, Hubei province, China. In early January, a novel betacoronavirus forming another clade within the subgenus sarbecovirus, now named SARS-CoV-2, was identified as the culprit of this disease currently being identified as "Coronavirus Disease 2019" (COVID-19) by WHO. Coronavirus was found to not only target the patient's lungs, but also multiple organs. Around 2-33% of COVID-19 patients developed gastrointestinal symptoms. Studies have shown that SAR-CoV-2 was found in patient's feces, suggesting that the virus can spread through feces. 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 million confirmed cases globally with 620 thousand deaths. Currently, there are more than 2000 confirmed cases of COVID-19 in Hong Kong. The investigators are uncertain about the impact of synbiotic on patients with COVID-19. However, a therapeutic strategy aiming at investigating the gut Imicrobiota of patients with COVID-9 who take synbiotic or not, leading to lesser progression to severe disease, less hospital stay and improved quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, Microbiota

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Health supplements + standard care
Arm Type
Active Comparator
Arm Description
28 days of health supplements (Synbiotic) daily plus standard care
Arm Title
Standard care
Arm Type
No Intervention
Arm Description
No intervention
Intervention Type
Other
Intervention Name(s)
Health supplements
Intervention Description
28 days of health supplements (synbiotic), 4g daily
Primary Outcome Measure Information:
Title
Combined symptom score
Description
Combined symptom score improvement of the first 4 weeks. Symptoms score assessment ranges from 20-80. The higher the score, the worse the symptoms.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Clinical improvement
Description
Compare the number and severity of symptoms existing by checking the list in symptoms assessment such as cough, shortness of breath, fever and gastrointestinal symptoms like anorexia, nausea, vomiting, abdominal pain, bloating before and during the study
Time Frame
4 weeks
Title
Time to develop antibody against SARS-CoV-2
Description
Compare the time to develop antibody against SARS-CoV-2 in both group
Time Frame
16 days
Title
Quality of life measured by EQ-5D-5L
Description
Improvement of quality of life measured by EQ-5D-5L. 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
4 weeks
Title
Quality of life measured by SF-12
Description
Improvement of quality of life measured by SF-12. 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
4 weeks
Title
Duration of hospital stay
Description
Measure the duration of hospital stay in both group
Time Frame
up to 3 months
Title
Time to negative PCR
Description
Compare the time to negative PCR in both group
Time Frame
through study completion, an average of 1 year
Title
Trend of symptom score
Description
Trend of symptom score, ranges from 26-104. The higher the score, the worse the symptoms.
Time Frame
4 weeks
Title
Gastrointestinal symptoms
Description
Duration of gastrointestinal symptoms such as anorexia, nausea, vomiting, abdominal pain, bloating within 4 week.
Time Frame
4 weeks
Title
Changes in fecal bacteria metabolites
Description
Changes in fecal bacteria metabolites measured by PCR at different time points
Time Frame
weeks 2, 4, 5 and 8 months 3, 6, 9 and 12
Title
Change in plasma cytokines level
Description
Change in plasma cytokines level at week 2 and week 5 compared with baseline
Time Frame
week 2 and week 5
Title
Changes in the gut microbiome
Description
Changes in the gut microbiome (bacteria, virome and fungome) measured by metagenomics at different time points (weeks 1, 2, 3, 4, 5 and months 3, 6, 9 and 12) compared to baseline
Time Frame
weeks 1, 2, 3, 4, 5, 8 and months 3, 6, 9 and 12
Title
Number of admission to Intensive Care Unit
Description
Number of admission to Intensive Care Unit
Time Frame
4 weeks
Title
Number of subjects with home discharge
Description
Number of subjects with home discharge
Time Frame
4 weeks
Title
Number of mortality
Description
Number of mortality
Time Frame
4 weeks
Title
Number of days absent from work
Description
Number of days absent from work since admission
Time Frame
3 months
Title
Change of quality of life questionnaire
Description
Change in score on Quality of life using EQ-5D-5L and SF-12. 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). While the 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
week 8, months 3, 6, 9 and 12
Title
Number of adverse event
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 at recruitment and that require admission to the hospitalization area; and Written informed consent is obtained Exclusion Criteria: Subjects admitted to Intensive Care Unit or on ventilator 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 history or active endocarditis Recent on CAPD or hemodialysis- Documented pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Siew Chien Ng
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Chinese University of Hong Kong
City
Sha Tin
ZIP/Postal Code
000000
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No
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An Evaluation of a Synbiotic Formula for Patients With COVID-19 Infection

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