The 2019 novel coronavirus (2019-nCoV) infection caused clusters of severe respiratory illness similar to SARS and was associated with ICU admission and high mortality. There is no confirmed antivirus therapy for people infected 2019-nCoV, most of them should receive supportive care to help relieve symptoms. This clinical trial is to evaluate the effect of Fuzheng Huayu tablet on lung inflammation in intensive patients with novel coronavirus pneumonia and reduce the progressive rate to critical type.
In December 2019, new coronavirus pneumonia (NCP) occurred in Wuhan, Hubei Province, which spread rapidly. Some of the patients developed into severe or critical illness. It became an international concerned public health emergencies and one of the major epidemics seriously endangering people's health and public safety after severe acute respiratory syndrome (SARS) in 2003. At present, we lack the specific treatment for NCP. The anti- novel coronavirus drugs are been conducting in clinical trials, and the other options includes the symptomatic treatment. The pathological mechanism of the disease is not clear, but due to the continuous development of inflammation, some cases can become severe or critical, which threatening the life and health of patients. Intensive cases with obvious inflammation, after the control of acute symptoms and signs, often have the performance of pulmonary fibrosis, affecting the recovery of lung function. Therefore, actively reducing lung inflammation, controlling and reversing pulmonary fibrosis is of great significance for the life and health of patients Infected novel coronavirus. Our previous study found that Fuzheng Huayu prescription can reduce the inflammation and fibrosis of the lung in the model rats, and improve the lung function of the patients with COPD. Therefore, we hope to take Fuzheng Huayu tablet to NCP patients, and observe whether it can reduce the lung inflammation of patients, so as to reduce the rate of progression of critical illness.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
66
Fuzheng Huayu tablet (0.4g/tablet, 1.6g/time, 3 times/day, oral; take medicine after meals each time)
Shuguang Hospital
Shanghai, Shanghai Municipality, China
the percentage of patients showing improvement in chest CT
Evaluation of the therapeutic effect of Fuzheng huayu tablet
Time frame: Week 2
remission rate or progression rate of critical illness
Evaluation of pulmonary inflammation improvement
Time frame: Week 2
clinical remission rate of respiratory symptoms
Evaluation of pulmonary inflammation improvement
Time frame: week 2
routine blood examination
Evaluation of pulmonary inflammation improvement
Time frame: Week 2
C-reactive protein level
Evaluation of the therapeutic effect of Fuzheng huayu tablet
Time frame: Week 2
procalcitonin level
Evaluation of pulmonary inflammation improvement
Time frame: Week 2
oxygen saturation
Evaluation of pulmonary inflammation improvement
Time frame: Week 2
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