Phase IIaTrials of GanMaoKangNing Granules

NCT ID: NCT02989012

Last Updated: 2016-12-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE2

Total Enrollment

96 participants

Study Classification

INTERVENTIONAL

Brief Summary

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Randomized, double-blind, double- simulation, positive drug-and-Placebo-Controlled, multicenter, phase IIa clinical trials Study about GanMaoKangNing Granules in improving the symptoms of influenza.

Detailed Description

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Conditions

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Epidemic Influenza

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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Drugs for experimental group

GanMaoKangNing Granules, blunted by boiled water , 3 times a day, 2 bags each time, for a course of five days(During experiments, The condition of the subjects sicker or complications, Whether need to change or increase the treatment measures were determined by the researchers ,Stop using the medicine , completion of the relevant inspection and evaluation after medication,Quit the test,the case according to the invalid qualified cases statistics.); Analogous Oseltamivir Phosphate Capsules,take oral,2 times a day,1 capsule each time, for a course of five days(During experiments, The condition of the subjects sicker or complications, Whether need to change or increase the treatment measures were determined by the researchers ,Stop using the medicine , completion of the relevant inspection and evaluation after medication,Quit the test,the case according to the invalid qualified cases statistics.).

Group Type EXPERIMENTAL

GanMaoKangNing Granules

Intervention Type DRUG

3 times a day, 2 bags each time.

Analogous Oseltamivir Phosphate Capsules

Intervention Type DRUG

2 times a day,1 capsule each time.

Drugs for control group

Oseltamivir Phosphate Capsules ,take oral,2 times a day,1 capsule each time, for a course of five days(During experiments, The condition of the subjects sicker or complications, Whether need to change or increase the treatment measures were determined by the researchers ,Stop using the medicine , completion of the relevant inspection and evaluation after medication,Quit the test,the case according to the invalid qualified cases statistics.); Analogous GanMaoKangNing Granules, blunted by boiled water , 3 times a day, 2 bags each time, for a course of five days(During experiments, The condition of the subjects sicker or complications, Whether need to change or increase the treatment measures were determined by the researchers ,Stop using the medicine , completion of the relevant inspection and evaluation after medication,Quit the test,the case according to the invalid qualified cases statistics.).

Group Type SHAM_COMPARATOR

Oseltamivir Phosphate Capsules

Intervention Type DRUG

2 times a day,1 capsule each time.

Analogous GanMaoKangNing Granules

Intervention Type DRUG

3 times a day, 2 bags each time.

Interventions

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GanMaoKangNing Granules

3 times a day, 2 bags each time.

Intervention Type DRUG

Analogous Oseltamivir Phosphate Capsules

2 times a day,1 capsule each time.

Intervention Type DRUG

Oseltamivir Phosphate Capsules

2 times a day,1 capsule each time.

Intervention Type DRUG

Analogous GanMaoKangNing Granules

3 times a day, 2 bags each time.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Sign the informed consent;
* Male and female patients aged between 18 and 65 years old , there is no limit on the gender;
* In line with the diagnostic criteria for pandemic influenza;
* Duration less than 48 (Duration is defined as the time from onset to test drugs for the first time before, the onset time pointed out that now the axillary temperature 38.0 ℃, headache, muscle or joint pain, chills, fatigue, cough, sore throat and a stuffy nose eight any flu symptoms and signs in time);
* The axillary temperature is 38.0 ℃ or higher;
* Nose and throat swabs rapid virus antigen test result is positive.

Exclusion Criteria

* Severe influenza and of patients with complications of influenza.
* With the following any severe risk factors:

A. With chronic respiratory diseases such as bronchial asthma, chronic obstructive pulmonary disease (copd), etc.

B. with chronic diseases of the cardiovascular system, such as congestive heart failure, high blood pressure.

C. with chronic metabolic and endocrine system diseases, such as poorly controlled diabetes (HbA1c 7.0% or higher).

D. with chronic kidney disease, chronic liver disease, blood system diseases, neurological and neuromuscular diseases (such as epilepsy, cognitive impairment, etc.).

E. A weakened immune system, such as long-term use of immunosuppressive agents, HIV infection or tumor.

F. Under the age of 19, long-term aspirin use. G. The obese (BMI BMI \> 30).

* With influenza complications, such as secondary bacterial pneumonia and other pathogenic bacteria and other viral pneumonia caused by pneumonia.
* A history of peptic ulcer disease or gastrointestinal bleeding.
* Into the group received within 48 h before flu antiviral treatment.
* Into the group of 12 months before been vaccinated against the flu.
* Into the group used within 2 weeks before the monoamine oxidase inhibitors.
* Blood leukocyte count \> 10.0 x 109 / L, neutrophils ratio \> 80%, or the need for systemic antibiotic therapy.
* For GanMaoKangNing Granules, Oseltamivir Phosphate Capsules, Acetaminophen Tablets, Dextromethorphan Hydrobromide Capsule, GanMaoKangNing Granules simulation agent or Oseltamivir Phosphate Capsules simulation agent composition of allergy, or allergic constitution.
* Aminotransferase (AST/SGOT) or alanine aminotransferase (ALT/SGPT) ≥ 1.5 x Upper Limit Normal (ULN), Scr \> Upper Limit Normal (ULN).
* Doubt or does have a history of alcohol or drug abuse.
* Pregnancy (defined as the pregnancy test positive), nursing mothers, or past in family planning.
* For nearly three months participated in other clinical trials of patients.
* Researchers think not appropriate to participate in this clinical subjects.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Dalian Zhen-Ao Bio-Tech Co., Ltd.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University

Beijing, Beijing Municipality, China

Site Status

Countries

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China

Facility Contacts

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Jing Wang Jing Wang, Dr.

Role: primary

Related Links

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http://www.who.int/mediacentre/factsheets/fs211/en/.

WHO. Influenza(Seasonal)\[EB/OL\].\[2015-12-31\]

Other Identifiers

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DalianZhen-Ao

Identifier Type: -

Identifier Source: org_study_id