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

Primary Purpose

Influenza

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
oseltamivir
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chinese medicinal herbs
oseltamivir and chinese medicinal herbs
Sponsored by
Capital Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Influenza focused on measuring Novel Influenza A(H1N1), Oseltamivir, Chinese Medicinal Herbs

Eligibility Criteria

14 Years - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Capital Medical University affiliated Beijing Chaoyang Hospital, Beijing Respiratory Medicine Insititute

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

blank

Oseltamivir

chinese medicinary herbs

oseltalmivir and chinese medicinal herbs

Arm Description

do not take antiviral therapy

antiviral therapy

antiviral therapy

combination antiviral therapy

Outcomes

Primary Outcome Measures

time to resolution of fever (the period from start of study-drug to relief of fever)

Secondary Outcome Measures

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

Full Information

First Posted
July 7, 2009
Last Updated
November 30, 2009
Sponsor
Capital Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT00935194
Brief Title
Chinese Medicinal Herbs Treatment on Novel Influenza A (H1N1) : Multi-centre, Prospective, Randomized Controlled Study
Official Title
Antiviral and Chinese Medicinal Herbs Treatment on Novel Influenza A (H1N1) Virus Infection: Multi-centre, Prospective, Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2009
Overall Recruitment Status
Completed
Study Start Date
July 2009 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Capital Medical University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza
Keywords
Novel Influenza A(H1N1), Oseltamivir, Chinese Medicinal Herbs

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
102 (Actual)

8. Arms, Groups, and Interventions

Arm Title
blank
Arm Type
Experimental
Arm Description
do not take antiviral therapy
Arm Title
Oseltamivir
Arm Type
Experimental
Arm Description
antiviral therapy
Arm Title
chinese medicinary herbs
Arm Type
Experimental
Arm Description
antiviral therapy
Arm Title
oseltalmivir and chinese medicinal herbs
Arm Type
Experimental
Arm Description
combination antiviral therapy
Intervention Type
Drug
Intervention Name(s)
oseltamivir
Other Intervention Name(s)
TamifluTM
Intervention Description
75mg,bid,for 5 days
Intervention Type
Other
Intervention Name(s)
blank
Intervention Description
no antiviral therapy
Intervention Type
Drug
Intervention Name(s)
chinese medicinal herbs
Intervention Description
200ml,p.o,qid,for 5 days
Intervention Type
Drug
Intervention Name(s)
oseltamivir and chinese medicinal herbs
Intervention Description
oseltamivir:75mg,p.o,bid,for 5 days; chinese medicinal herbs:200ml,p.o,qid,for 5 days
Primary Outcome Measure Information:
Title
time to resolution of fever (the period from start of study-drug to relief of fever)
Time Frame
one year
Secondary Outcome Measure Information:
Title
time to resolution of respiratory symptoms(defined as the period from start of study-drug to relief of symptoms)
Time Frame
one year
Title
virus shedding time
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chen Wang, Doctor
Organizational Affiliation
Capital Medical University affiliated Beijing Chaoyang Hospital, Beijing Respiratory Medicine Insititute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Qingquan Liu, Docter
Organizational Affiliation
Beijing Chinese Traditional Medicine University affiliated Dongzhimen Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yu Mao, Doctor
Organizational Affiliation
Beijing Ditan Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Capital Medical University affiliated Beijing Chaoyang Hospital, Beijing Respiratory Medicine Insititute
City
Beijing
ZIP/Postal Code
100020
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
21844547
Citation
Wang C, Cao B, Liu QQ, Zou ZQ, Liang ZA, Gu L, Dong JP, Liang LR, Li XW, Hu K, He XS, Sun YH, An Y, Yang T, Cao ZX, Guo YM, Wen XM, Wang YG, Liu YL, Jiang LD. Oseltamivir compared with the Chinese traditional therapy maxingshigan-yinqiaosan in the treatment of H1N1 influenza: a randomized trial. Ann Intern Med. 2011 Aug 16;155(4):217-25. doi: 10.7326/0003-4819-155-4-201108160-00005. Erratum In: Ann Intern Med. 2012 Jan 3;156(1 Pt 1):71.
Results Reference
derived

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

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