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Effects of Multivitamin Supplementation on Upper Respiratory Tract Infection in Chinese adults: A (pilot) Retrospective Study

Effects of Multivitamin Supplementation on Upper Respiratory Tract Infection in Chinese adults: A (pilot) Retrospective Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074204
Enrollment
Unknown
Registered
2023-08-01
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-08-07

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

Conditions

Upper Respiratory Tract Infection

Interventions

Control group (No multivitamin mineral tablets):NA
The research group (Take multivitamin and mineral tablets for 3 months or more):NA

Sponsors

Sun Yat-Sen Memorial Hospital Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: -=18 years -Health care professionals and/or general population taking/not taking multivitamin tablets (Any Centrum multivitamin product) with at least 4 days per week and continuous supplementation for at least 3 months prior to the onset of infection. For example, to observe the endpoint of SARS-CoV-2 infection starts from early 15th December, 2022, participants should at least consecutively take multivitamin supplementation between early 13th September 2022 and 14thDecember 2022. -Able to understand the questionnaire and can provide clear start and end date of infection, duration and severity of symptoms, medications. Good compliance, able to cooperate with questionnaire survey and follow-up.

Exclusion criteria

Exclusion criteria: -Subjects with autoimmune disease and compromised immunity or on medication that can affect immune function -Pregnant or lactating women -Concurrently take other (multi)vitamins or minerals, protein powders or other nutritional supplements that can affect immunity -Participated in other drug clinical trials during investigation Mental impairment, unable to understand the nature, significance and expected consequences of the research, and/or with uncooperative attitude

Design outcomes

Primary

MeasureTime frame
COVID-19 infection;

Secondary

MeasureTime frame
Incidence rate and severity of Upper respiratory tract infection;Incidence rate of SARS CoV-2 infection;

Countries

China

Contacts

Public ContactChaogang Chen

Sun Yat-Sen Memorial Hospital Sun Yat-Sen University

ccg2002@163.com+86 189 2218 2885

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026