Selected article for: "clinical endpoint and current study"

Author: Feng, Jun; Zhou, Shuang; Xie, Qin; Huang, Tingrong; Xu, Xiaoming; Zhou, Daixing; Zhang, Wen; Sun, Shuting; Liu, Xudong; Wu, Xinxin; Che, Jinhua; Fan, Tian; Zou, Dengxiu; Wang, Junshuai; Zhan, Daqian; Peng, Dan; Feng, Yikuan; Yu, Gang; Yuan, Zuobiao; Fang, Bangjiang
Title: Traditional Chinese Medicine Shenhuang Granule in Patients with Severe/Critical COVID-19: A Randomized Controlled Multicenter Trial
  • Cord-id: tlrh7ew6
  • Document date: 2021_5_28
  • ID: tlrh7ew6
    Snippet: BACKGROUND: Coronavirus disease 2019 (COVID-19) is still a pandemic, with a high mortality rate in severe/critical cases. Therapies based on the Shenghuang Granule have proved helpful in viral infection and septic shock. HYPOTHESIS/PURPOSE: The objective of the current study was to compare the efficacy and safety of the traditional Chinese medicine, Shenhuang Granule, with standard care in hospitalized patients with severe/critical COVID-19. STUDY DESIGN AND METHODS: This was an open-label, mult
    Document: BACKGROUND: Coronavirus disease 2019 (COVID-19) is still a pandemic, with a high mortality rate in severe/critical cases. Therapies based on the Shenghuang Granule have proved helpful in viral infection and septic shock. HYPOTHESIS/PURPOSE: The objective of the current study was to compare the efficacy and safety of the traditional Chinese medicine, Shenhuang Granule, with standard care in hospitalized patients with severe/critical COVID-19. STUDY DESIGN AND METHODS: This was an open-label, multicenter, randomized, controlled clinical trial. At 4 medical centers, a total of 111 severe/critical patients were randomly assigned to receive Shenhuang Granule (SHG group) twice a day for 14 days, in addition to standard care, or to receive standard care alone (Control group). The maximal follow up time was 75 days. The clinical endpoint was clinical improvement and mortality. RESULTS: 54 patients were assigned to the control group and 57 to the SHG group. The overall mortality was 75.9% (41/54) in the control group, and 38.6% (22/57) in the SHG group (p<0.01 vs control). The post hoc analysis showed that in the severe category, the mortality of the control group vs. the SHG group was 58.8% (10/17) vs 5.3% (1/19) (p<0.01); while in the critical category, it was 83.8% (31/37) vs. 55.3% (21/38) (p<0.05). In the severe category, the mortality of patients who eventually received an invasive ventilator in the control vs. the SHG group was 58.8% (10/17) vs. 0 (0/19) (p<0.01). Administration of SHG was associated with increased lymphocytes and decreased adverse events. CONCLUSION: Shenhuang Granule is a promising integrative therapy for severe and critical COVID-19.

    Search related documents:
    Co phrase search for related documents
    • abdominal disease and liver dysfunction: 1
    • abdominal disease and long follow: 1
    • active case and acute inflammation: 1
    • active case and acute leukemia: 1, 2, 3
    • acute disorder and liver dysfunction: 1
    • acute inflammation and liver dysfunction: 1
    • acute inflammation and long follow: 1
    • acute inflammation and lung tumor: 1, 2, 3
    • acute inflammation and lymphocyte count: 1, 2, 3, 4, 5, 6, 7, 8
    • acute leukemia and liver dysfunction: 1
    • acute leukemia and long follow: 1, 2
    • acute leukemia and lymphocyte count: 1, 2
    • acute upper respiratory tract infection and lymphocyte count: 1, 2
    • admission status and long follow: 1
    • admission status and lymphocyte count: 1, 2, 3, 4, 5
    • live discharge and lymphocyte count: 1
    • liver dysfunction and lymphocyte count: 1, 2, 3
    • long follow and lung tumor: 1, 2
    • long follow and lymphocyte count: 1, 2, 3