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Phase IIaTrials of GanMaoKangNing Granules

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02989012
Enrollment
96
Registered
2016-12-12
Start date
Unknown
Completion date
Unknown
Last updated
2016-12-12

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

Conditions

Epidemic Influenza

Brief summary

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.

Interventions

DRUGGanMaoKangNing Granules

3 times a day, 2 bags each time.

DRUGAnalogous Oseltamivir Phosphate Capsules

2 times a day,1 capsule each time.

2 times a day,1 capsule each time.

DRUGAnalogous GanMaoKangNing Granules

3 times a day, 2 bags each time.

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Flu recovery timesix daysAll the time needed for symptoms eased that from medication to fever and headache, muscle joint pain, chills, fatigue, cough, sore throat and a stuffy nose.

Secondary

MeasureTime frameDescription
Single symptom remission ratesix daysAfter the medication and three days later, The proportion of each individual symptoms of subjects which include of headache, muscle joint pain, chills, fatigue, cough, sore throat and a stuffy nose. Symptoms defined as symptom scores dropped to 0 or 1 minute, and maintain for 24 h or more.
The antifebrile effectsix daysAntifebrile rate: After the medication and three days later, the percentage of Body temperature returned to normal subjects (the axillary temperature \< 37.1 ℃, and maintain of 24 h or more time). Medicine antifebrile time (h) : Medication for the first time to the axillary temperature \< 37.1 ℃, and maintain of 24 h or more time.

Other

MeasureTime frameDescription
The conditions of drug utilization of the antipyretic and some cough medicinesix daysIncluding acetaminophen tablets and capsule of dextromethorphan hydrobromide usage rate and dose.

Countries

China

Outcome results

None listed

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