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Evaluation of a Synbiotic Formula in Patient With COVID-19

Evaluation of a Synbiotic Formula in Patient With COVID-19

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04730284
Enrollment
20
Registered
2021-01-29
Start date
2020-08-25
Completion date
2022-03-31
Last updated
2021-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronavirus

Keywords

microbiota

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.

Interventions

tailor-made Synbiotics, 4g per day for 28 days

Sponsors

Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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 and released from isolation at recruitment. 3. Written informed consent obtained

Exclusion criteria

1. Known allergy or intolerance to the intervention product or its components 2. 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) 3. 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 4. 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 5. Documented pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Changes in gut microbiomeweek 5Changes in the gut microbiome (bacteria, virome and fungome) measured by metagenomics at week 5 compared to baseline

Secondary

MeasureTime frameDescription
Change in plasma cytokines including IL-6, IL-IB, TNF-a and CXCL-10week 5Change in plasma cytokines level at week 5 compared with baseline
Trend in symptom scoreweeks 2, 4, 5, 8 and months 3, 6, 9 and 12Trend 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-5Lweeks 2, 4, 5, 8 and months 3, 6, 9 and 12Change 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).
Changes in fecal bacteria metabolitesweeks 2, 4, 5, 8 and months 3, 6, 9 and 12Changes in fecal bacteria metabolites by PCR at different time points
Change in Quality of life measured by SF-12weeks 2, 4, 5, 8 and months 3, 6, 9 and 12Change 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.
Adverse event assessment3 monthsNumber of adverse event
Duration of gastrointestinal symptoms4 weeksDuration of gastrointestinal symptoms such as anorexia, nausea, vomiting, abdominal pain, bloating within 4 weeks.

Countries

Hong Kong

Contacts

Primary ContactKristy Ho, Bsc
hiutungho@cuhk.edu.hk85235053855
Backup ContactKitty Cheung, MPH
kittyccy@cuhk.edu.hk85226373225

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026