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A Post-marketing Research on Jinyebaidu Granule in Treating Patients With Acute Upper Respiratory Infection

Primary Purpose

Acute Upper Respiratory Infection

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Jinyebaidu granule
Fufangshuanghua granule
Jinyebaidu granule placebo
Fufangshuanghua granule placebo
Sponsored by
China Academy of Chinese Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Upper Respiratory Infection

Eligibility Criteria

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

Inclusion Criteria

  • Patients diagnosed as acute upper respiratory infection.
  • Patients with acute upper respiratory infection diagnosed as Traditional Chinese Medicine(TCM) syndrome wind-heat attacking the Lung (type of heat pathogen invading the defensive Qi of the lung).
  • Acute upper respiratory infection onset time is less than 36 hours.
  • Patients aged 18 to 70 years old.
  • Patients agreed to participate this study and sign the informed consent.

Exclusion Criteria:

  • Patients diagnosed with suppurative tonsillitis (third degree), and chest X-ray imaging showed lung inflammation;
  • White blood cell counts more than 12 E9, neutrophils more than 80%, ALT, AST, BUN, Cr more than 2 times of the normal upper limit;
  • Patients with temperature lower than 37.5 degree centigrade, and without sore throat;
  • Patients with temperature higher than 38.5 degree centigrade;
  • Patients already receiving antibiotics or other similar drug treatment;
  • Patients associated with other severe primary lung diseases, such as lung cancer, tuberculosis, pneumonia and other infectious diseases;
  • Patients complicated with cardiovascular and cerebrovascular diseases, severe primary diseases of hematopoietic system, mental illness;
  • Pregnant or lactating women;
  • Patients with immunodeficiency resulted from organ transplantation, HIV / AIDS, or long-term use of immunosuppressive agents;
  • Patients with drug allergy;
  • Patients participating in other clinical trials, which influence outcome evaluation of the research.

Sites / Locations

  • Guang'anmen HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Treatment group

Control group

Arm Description

Jinyebaidu granule, blunt, 10g / time, three times a day; Fufangshuanghua granule placebo, blunt, 6g / time, 4 times a day.

Fufangshuanghua granule, blunt, 6g / time, 4 times a day; Jinyebaidu granule placebo, blunt, 10g / times, three times a day.

Outcomes

Primary Outcome Measures

The time to defervescence

Secondary Outcome Measures

Change of symptoms score
The symptoms includes sore throat, cough, expectoration, headache, thirst. According to severity ,each symptom include four grades. The scores of sore throat are 0,2,4,6. The scores of cough, expectoration ,headache, thirst are 0,1,2,3. Compare the change from baseline all of symptoms score at the third day and at the fifth day. References: Mao bing, Li ting-qian, Li ming-quan, Tu jin-wen, Zhang rui-ming, et al. Clinical randomized double--blinded observation on effect of Jinyebaidu Granule in treating the disease of wind-heat attacking the lung(type of heat pathogen invading the defensive Qi of the lung). chinese JounIal of Evidence-Based Medicine Jun, 2003,3(2):115-120
Change of signs score
The signs includes swollen tonsils and pharyngeal hyperemia. According to severity, each sign includes four grades. The scores are 0,4,6,8. References: Mao bing, Li ting-qian, Li ming-quan, Tu jin-wen, Zhang rui-ming, et al. Clinical randomized double--blinded observation on effect of Jinyebaidu Granule in treating the disease of wind-heat attacking the lung(type of heat pathogen invading the defensive Qi of the lung). chinese JounIal of Evidence-Based Medicine Jun, 2003,3(2):115-120
Adverse events
Change of routine blood test
The routine blood test includes white blood cell count, neutral cell ratio, lymphocyte ratio, single nuclear cell ratio, red blood cell count, hemoglobin, platelet count
Change of urine routine
The urine routine includes white blood cell count, red blood cell count,urine protein,urine sugar
Change of liver function
The liver function includes glutamic-pyruvic transaminase,glutamic-oxalacetic transaminase
Change of renal function
The renal function includes creatinine,usea nitrogen
Incidence of ECG abnormalities

Full Information

First Posted
April 18, 2015
Last Updated
September 2, 2015
Sponsor
China Academy of Chinese Medical Sciences
Collaborators
First Affiliated Hospital of Heilongjiang Chinese Medicine University, Guang'anmen Hospital of China Academy of Chinese Medical Sciences, Beijing Hospital of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Liaoning University of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Guangdong Provincial Hospital of Traditional Chinese Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT02539277
Brief Title
A Post-marketing Research on Jinyebaidu Granule in Treating Patients With Acute Upper Respiratory Infection
Official Title
A Post-marketing Research on Jinyebaidu Granule in Treating Patients With Acute Upper Respiratory Infection: A Double Blind, Double Dummy, Randomized, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Unknown status
Study Start Date
December 2014 (undefined)
Primary Completion Date
November 2015 (Anticipated)
Study Completion Date
November 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
China Academy of Chinese Medical Sciences
Collaborators
First Affiliated Hospital of Heilongjiang Chinese Medicine University, Guang'anmen Hospital of China Academy of Chinese Medical Sciences, Beijing Hospital of Traditional Chinese Medicine, Changchun University of Chinese Medicine, Liaoning University of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Guangdong Provincial Hospital of Traditional Chinese Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Study topic:A comparative effectiveness research on Jinyebaidu granule in treating patients with acute upper respiratory infection: A double blind, double dummy, randomized, controlled trial. It is a post-marketing clinical study to evaluate effectiveness, safety and cost-effectiveness on Jinyebaidu granule in treating acute upper respiratory infection. Objectives of Study:This study aims to evaluate effectiveness, safety and cost-effectiveness on Jinyebaidu granule in treating patients with acute upper respiratory infection. Study design:multi-center double-blind, double-dummy, randomized, controlled trial
Detailed Description
Inclusion criteria Patients diagnosed as acute upper respiratory infection. Patients with acute upper respiratory infection diagnosed as Traditional Chinese Medicine(TCM) syndrome wind-heat attacking the Lung (type of heat pathogen invading the defensive Qi of the lung). Acute upper respiratory infection onset time is less than 36 hours. Patients aged 18 to 70 years old. Patients agreed to participate this study and sign the informed consent. Effectiveness evaluation TCM symptoms: fever, sore throat, cough with or without expectoration, headache, thirst, change of tongue body, tongue coating and pulse. Signs: swollen tonsils, pharyngeal hyperemia. Body temperature Safety evaluation Clinical symptoms and signs of adverse event reaction Signs: blood pressure, respiration, heart rate, body temperature; Routine blood test and urine routine; Liver function and renal function: Alanine transaminase (ALT)、glutamic-oxalacetic transaminease(AST)、serum creatinine(SCr)、urea nitrogen(BUN) ; Incidence of electrocardiogram(ECG) abnormalities. Cost-effectiveness evaluation cost calculation The direct medical costs include: the registration expenses, examination expenses, laboratory test expenses, Treatment costs, Chinese medicine expenses, Chinese herbal medicine expenses, western medicine expenses; Indirect medical costs: transportation costs, lost income patients; Adverse drug reactions cost: the cost of treatment due to adverse drug reactions. Effect Evaluation:Symptoms and signs score, physical examination, the incidence of complications. Number of participants 600 participants will be divided into two groups, the experimental group (n=300)and the control group (n=300).Each group will be stratified into three layers according to fever, sore throat, fever and sore throats. 100 patients will be included in each level. Dose regimen treatment group: Jinyebaidu granule, blunt, 10g/time, three times a day; Compound Shuanghua granules placebo, blunt, 6g /time, 4 times a day. Control group: Compound double flowers particles, blunt, 6g/time, 4 times a day; Jinyebaidu Granule placebo, blunt, 10g/time, three times a day. Course of treatment:5 days

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Upper Respiratory Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment group
Arm Type
Experimental
Arm Description
Jinyebaidu granule, blunt, 10g / time, three times a day; Fufangshuanghua granule placebo, blunt, 6g / time, 4 times a day.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Fufangshuanghua granule, blunt, 6g / time, 4 times a day; Jinyebaidu granule placebo, blunt, 10g / times, three times a day.
Intervention Type
Drug
Intervention Name(s)
Jinyebaidu granule
Intervention Description
It is a chinese patent medicine extracted from four herbs: honeysuckle, isatis leaf, dandelion, and houttuynia cordata thunb.
Intervention Type
Drug
Intervention Name(s)
Fufangshuanghua granule
Intervention Description
It is a Chinese patent medicne extracted from four herbs: honeysuckle, forsythia, radix Isatidis, andrographis paniculata.
Intervention Type
Drug
Intervention Name(s)
Jinyebaidu granule placebo
Intervention Description
It is Jinyebaidu granule placebo.
Intervention Type
Drug
Intervention Name(s)
Fufangshuanghua granule placebo
Intervention Description
It is Fufangshuanghua granule placebo.
Primary Outcome Measure Information:
Title
The time to defervescence
Time Frame
defined as the time from the first dose of study medication to the time when the body temperature declined to lower than 37.3ºC
Secondary Outcome Measure Information:
Title
Change of symptoms score
Description
The symptoms includes sore throat, cough, expectoration, headache, thirst. According to severity ,each symptom include four grades. The scores of sore throat are 0,2,4,6. The scores of cough, expectoration ,headache, thirst are 0,1,2,3. Compare the change from baseline all of symptoms score at the third day and at the fifth day. References: Mao bing, Li ting-qian, Li ming-quan, Tu jin-wen, Zhang rui-ming, et al. Clinical randomized double--blinded observation on effect of Jinyebaidu Granule in treating the disease of wind-heat attacking the lung(type of heat pathogen invading the defensive Qi of the lung). chinese JounIal of Evidence-Based Medicine Jun, 2003,3(2):115-120
Time Frame
change from baseline symptoms score at the third day and at the fifth day
Title
Change of signs score
Description
The signs includes swollen tonsils and pharyngeal hyperemia. According to severity, each sign includes four grades. The scores are 0,4,6,8. References: Mao bing, Li ting-qian, Li ming-quan, Tu jin-wen, Zhang rui-ming, et al. Clinical randomized double--blinded observation on effect of Jinyebaidu Granule in treating the disease of wind-heat attacking the lung(type of heat pathogen invading the defensive Qi of the lung). chinese JounIal of Evidence-Based Medicine Jun, 2003,3(2):115-120
Time Frame
change from baseline signs score at the fifth day
Title
Adverse events
Time Frame
All the time in the study
Title
Change of routine blood test
Description
The routine blood test includes white blood cell count, neutral cell ratio, lymphocyte ratio, single nuclear cell ratio, red blood cell count, hemoglobin, platelet count
Time Frame
Change from base line, on the fifth day
Title
Change of urine routine
Description
The urine routine includes white blood cell count, red blood cell count,urine protein,urine sugar
Time Frame
Change from base line, on the fifth day
Title
Change of liver function
Description
The liver function includes glutamic-pyruvic transaminase,glutamic-oxalacetic transaminase
Time Frame
Change from base line, on the fifth day
Title
Change of renal function
Description
The renal function includes creatinine,usea nitrogen
Time Frame
Change from base line, on the fifth day
Title
Incidence of ECG abnormalities
Time Frame
Change from base line, on the fifth day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients diagnosed as acute upper respiratory infection. Patients with acute upper respiratory infection diagnosed as Traditional Chinese Medicine(TCM) syndrome wind-heat attacking the Lung (type of heat pathogen invading the defensive Qi of the lung). Acute upper respiratory infection onset time is less than 36 hours. Patients aged 18 to 70 years old. Patients agreed to participate this study and sign the informed consent. Exclusion Criteria: Patients diagnosed with suppurative tonsillitis (third degree), and chest X-ray imaging showed lung inflammation; White blood cell counts more than 12 E9, neutrophils more than 80%, ALT, AST, BUN, Cr more than 2 times of the normal upper limit; Patients with temperature lower than 37.5 degree centigrade, and without sore throat; Patients with temperature higher than 38.5 degree centigrade; Patients already receiving antibiotics or other similar drug treatment; Patients associated with other severe primary lung diseases, such as lung cancer, tuberculosis, pneumonia and other infectious diseases; Patients complicated with cardiovascular and cerebrovascular diseases, severe primary diseases of hematopoietic system, mental illness; Pregnant or lactating women; Patients with immunodeficiency resulted from organ transplantation, HIV / AIDS, or long-term use of immunosuppressive agents; Patients with drug allergy; Patients participating in other clinical trials, which influence outcome evaluation of the research.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Junjie Jiang, doctor
Phone
86-18910206360
Email
studentjiangjunjie@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yuan Li, bachelor
Email
zyly890609@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yanming Xie
Organizational Affiliation
Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences
Official's Role
Study Chair
Facility Information:
Facility Name
Guang'anmen Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100053
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wensheng Qi

12. IPD Sharing Statement

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A Post-marketing Research on Jinyebaidu Granule in Treating Patients With Acute Upper Respiratory Infection

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