The Efficacy and Safety Study of Fuganlin Oral Liquid in Children With Influenza (Acute Upper Respiratory Infection)
Launched by GUANGZHOU YIPINHONG PHARMACEUTICAL CO.,LTD · Dec 3, 2015
Trial Information
Current as of May 21, 2025
Completed
Keywords
ClinConnect Summary
Treatment group: Fuganlin Oral Liquid 10mL. Control group: Xiaoer Jiebiao oral liquid 100mL. Treatment for one week. Patients who were recovered within one week can withdrawal at any time.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients diagnosed as acute upper respiratory infection.
- • 2. Patients with Traditional Chinese Medicine syndrome of qi deficiency and wind-heat.
- • 3. Patients aged 1 to 12 years.
- • 4. With course of disease in 48 hours or less.
- • 5. Signed informed consent by a Parent or legal guardians.
- Exclusion Criteria:
- • 1. Patients diagnosed as tonsillitis, bronchitis, bronchiolitis, pneumonia;
- • 2. Patients have a history of hyperpyretic convulsion;
- • 3. Severe malnutrition, rickets patients and merge the heart, brain, liver, kidney and hematopoietic system and other serious primary diseases;
- • 4. The increased of serum creatinine (Cr), blood urea nitrogen (BUN), alanine aminotransferase (ALT), and urinary protein, urine RBC above "+", which can not use the test illness or possibly combined disease conditions to explain;
- • 5. Patients with allergic physique (Allergic to above two kinds of substance), allergic to the composition of the preparation or control drug;
- • 6. According to the doctors' determination,likely to loss to follow up.
About Guangzhou Yipinhong Pharmaceutical Co.,Ltd
Guangzhou Yipinhong Pharmaceutical Co., Ltd. is a leading pharmaceutical company based in Guangzhou, China, dedicated to the research, development, and commercialization of innovative healthcare solutions. With a strong focus on quality and efficacy, the company specializes in a diverse range of therapeutic areas, including oncology, cardiology, and infectious diseases. Yipinhong is committed to advancing medical science through robust clinical trials and collaborations, ensuring that patients have access to safe and effective treatments. The company's mission is to enhance global health outcomes by leveraging cutting-edge technology and adhering to the highest regulatory standards in the pharmaceutical industry.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Luohe, Henan, China
Patients applied
Trial Officials
Cao xia, MD
Principal Investigator
Chongqing First People's Hospital
Yan yunying, MD
Principal Investigator
Nanning maternal and Child Health Hospital
Hu suping, MD
Principal Investigator
Nanchang City Hospital of integrated traditional Chinese and Western Medicine
Wang leping, MD
Principal Investigator
Changzhou traditional Chinese medicine hospital
Liu Dexing, MD
Principal Investigator
Liuzhou traditional Chinese medicine hospital
Qi Shihe, MD
Principal Investigator
Xiangyang Central Hospital
Ding Lijun, MD
Principal Investigator
Handan traditional Chinese medicine hospital
Yang Liping, MD
Principal Investigator
Changzhi City People's Hospital
Feng Ziwei, MD
Principal Investigator
Luohe traditional Chinese medicine hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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