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Chinese Medicinal Herbs Treatment on Novel Influenza A (H1N1) : Multi-centre, Prospective, Randomized Controlled Study

Antiviral and Chinese Medicinal Herbs Treatment on Novel Influenza A (H1N1) Virus Infection: Multi-centre, Prospective, Randomized Controlled Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00935194
Enrollment
102
Registered
2009-07-08
Start date
2009-07-31
Completion date
2009-11-30
Last updated
2009-12-01

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

Conditions

Influenza

Keywords

Novel Influenza A(H1N1), Oseltamivir, Chinese Medicinal Herbs

Brief summary

The purpose of this study is to determine whether Chinese medicinal herbs are effective and safe for treating novel influenza A (H1N1) infection.

Detailed description

The antiviral agent, oseltamivir, is recommended by the World Health Organization (WHO) to treat recent outbreak novel influenza A (H1N1) virus infection around world. But limited stock and resistant strain emergence raised increasing concerns. Chinese medicinal herbs, are derived from plants and usually incorporate one or more herbs as the basic drug(s) to treat the disease. The investigators performed RCT to indicate that Chinese medicinal herbs was effective and safe for treating novel influenza A (H1N1) infection.

Interventions

DRUGoseltamivir

75mg,bid,for 5 days

OTHERblank

no antiviral therapy

DRUGchinese medicinal herbs

200ml,p.o,qid,for 5 days

oseltamivir:75mg,p.o,bid,for 5 days; chinese medicinal herbs:200ml,p.o,qid,for 5 days

Sponsors

Capital Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
14 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Confirmed novel influenza A(H1N1) case with laboratory evidence * 70 years ≥ age ≥ 14years * Within 72hr after the onset of symptoms(body temperature≥37.5℃ with at least one respiratory symptom (cough, sore throat, or nasal symptom)

Exclusion criteria

* Age \< 14 years or \> 70 years * Bronchitis, pneumonia, pleural fluid and interstitial infiltration showed by Chest radiology(x-ray or CT) * Severe chronic underlying diseases: severe COPD(FEV1/EVC \<70% and FEV1 \<30% predicted or respiratory failure or congestive heart failure), severe hepatic disfunction(ALT or AST ≥3 times normal elevation), renal disfunction(Cr\>2mg/dL), chronic heart failure(NYHA Ⅲ-Ⅳ grade) * Immunocompromised patients(cancer, organ transplant, AIDS and a history of treatment with immunosuppressive drug and glucocorticoids in the past 3 months) * Taken Chinese medicinal herbs, antiviral or antibiotic drug in the past 2 weeks * Inoculation influenza vaccination * One of the following items appeared at the enrollment * respiratory failure:PaO2\<60mmHg and/or PCO2\>50mmHg or PaO2/FiO2≤300 * circulation failure: despite adequate fluid resuscitation and cardiac output, systolic \<90mmHg or requirement inotropic support * renal function failure: despite adequate fluid resuscitation and cardiac output, urine ≤ 0.5ml/kg.h, Cr or BUN≥1 time normal elevation * hepatic function failure: total bilirubin\>34μmol/L or ALT/AST ≥3 times normal - Other unappropriated enrollment situations considered by investigator

Design outcomes

Primary

MeasureTime frame
time to resolution of fever (the period from start of study-drug to relief of fever)one year

Secondary

MeasureTime frame
time to resolution of respiratory symptoms(defined as the period from start of study-drug to relief of symptoms)one year
virus shedding timeone year

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026