Skip to content

The Effect of Synbiotics on the Upper Respiratory Tract Infection

The Effect of Synbiotics on the Upper Respiratory Tract Infection in Healthy Subjects: A Randomized Double-Blind Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04960878
Enrollment
58
Registered
2021-07-14
Start date
2020-10-05
Completion date
2021-01-05
Last updated
2021-07-14

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

Conditions

Gut Microbiota, Immune Function, Upper Respiratory Tract Infection

Brief summary

Gut microbiome manipulation to alter the gut-lung axis may potentially protect humans against respiratory infections. However, clinical trials of synbiotics, one of the microbiota-targeted intervention, in this regard is few. Therefore, this study aims to examine the effect of synbiotics on the incidence and severity of upper respiratory tract infection, gut microbiota composition and function, as well as biomarkers of immune function.

Interventions

DIETARY_SUPPLEMENTSynbiotic

Synbiotics sachet mainly contained Lactobacillus rhamnosus HN001, Bifidobacterium lactis HN019, and fructooligosaccharides.

DIETARY_SUPPLEMENTPlacebo

Maltodextrin

Sponsors

Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* aged 18-65 years; * good general health as determined by medical questionnaires; * BMI \<35 kg/m2;

Exclusion criteria

* known congenital or acquired immune defects; * allergies and other chronic or acute diseases requiring treatment; * subjects with chronic gastrointestinal diseases; * alcohol or drug misuse or both; * pregnancy or lactation; * vaccination against influenza within the last 12 months; * use of oral antibiotics, probiotics, prebiotics, synbiotics, drugs active on gastrointestinal motility, or a laxative of any class within the last month.

Design outcomes

Primary

MeasureTime frame
The incidence of the upper respiratory tract infectionUp to 8 weeks

Secondary

MeasureTime frameDescription
The duration of the upper respiratory tract infectionUp to 8 weeks
The severity of the upper respiratory tract infectionUp to 8 weeksThe severity of the upper respiratory tract infection was assessed using the 24-item Wisconsin Upper Respiratory Symptom Survey (WURSS-24). Paricipants were required to answer the question, Did you have any symptom of upper respiratory tract infection today? If someone answered yes, he/she was instructed to complete WURSS-24 surveys daily.
Changes in the gut mictobiotaBaseline, 4 weeks, 8 weeksChanges in the composition, diversity, and function of gut mictobiota in feces will be measured by 16S rRNA gene sequencing.
Changes in the levels of sIgA in saliva and fecesBaseline, 4 weeks, 8 weeks
Changes in the levels of inflammatory cytokineBaseline, 4 weeks, 8 weeksChanges in the levels of fasting plasma inflammatory cytokine, including CRP, IL-1β, IL-6, IL-8, IL-10, TNF-α, and IFN-γ.
Changes in the number of T, B, NK and monocytes populationsBaseline, 4 weeks, 8 weeksChanges in the number of T-lymphocytes(CD45+CD3+), B-lymphocytes(CD45+CD19+), monocytes(CD45+CD14+), and natural killer cells(CD45+CD56+) in blood samples were evaluated by flow cytometer.
Changes in the subpopulation frequencies of blood lymphocyte and dendritic cellsBaseline, 4 weeks, 8 weeksChanges in the subpopulation of blood lymphocytes (the levels of CD3+, CD4+, CD8+, and CD25+) and dendritic cells (the levels of CD3-CD19-CD56-HLA-DR+ CD11c+cells and CD3-CD19-CD56-HLA-DR+CD123+ cells ) in blood samples were evaluated by flow cytometer.
Change in body weightBaseline, 4 weeks, 8 weeks
Change in BMIBaseline, 4 weeks, 8 weeks
Change in body fat compositionBaseline, 4 weeks, 8 weeks
Change in the levels fasting plasma glucoseBaseline, 4 weeks, 8 weeks
Changes in the levels of fasting plasma TC, TG, LDL, and HDLBaseline, 4 weeks, 8 weeks

Countries

China

Outcome results

None listed

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