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The Impact of Vitamin on the Clinical Course in Cases Infected by Novel H1N1 Influenza Virus A

The Impact of Vitamin on the Clinical Course in Cases Infected by Novel H1N1 Influenza Virus A: a Randomized-controlled Trial

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01127282
Enrollment
180
Registered
2010-05-20
Start date
2009-12-31
Completion date
2010-08-31
Last updated
2010-05-20

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

Conditions

H1N1 Influenza

Keywords

influenza, vitamin, improvement of symptom

Brief summary

Influenza continues to inflict an important burden on health-care systems. The 2009 H1N1 influenza virus first appeared in Mexico and the United States in March and April 2009 and has swept the globe with unprecedented speed. The aim of this study is to evaluate effect of supplement vitamin on the clinical course of patients with acute respiratory illness suspected novel H1N1 infection.

Detailed description

Patients with acute respiratory illness randomized to control or vitamin groups. The patients completed questionnaire about their initial symptom scores. After 5 days of vitamin trial, patients were asked about their symptom by telephone survey.

Interventions

DRUGVitamin (vitamin A 15 mg,C 500 mg, E 400IU)

Vitamin (vitamin A 15 mg,C 500 mg, E 400IU) 1T po for 5 days in addition to anti-viral agent and antipyretics

DRUGPlacebo (digestive tablet)

Placebo (digestive tablet) 1T po for 5 days in addition to anti-viral agent and antipyretics

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

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

Inclusion criteria

* Age \> 20 years * Acute respiratory illness suspected H1N1 infection * Acute febrile respiratory illness(BT \> 37.8) and throat pain or cough or nasal congestion

Exclusion criteria

* Pregnancy * Hypersensitivity to vitamin A * History of liver disease or renal disease * Urinary stone disease

Design outcomes

Primary

MeasureTime frame
change of symptom score1 week after initial visit

Countries

South Korea

Contacts

Primary ContactChang-Hoon Lee, MD
kauri670@gmail.com+82- 2- 870- 2232
Backup ContactJong Sun Park, MD
jspark.im@gmail.com

Outcome results

None listed

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