Selected article for: "observation follow period and safety treatment efficacy"

Author: He, Jiayang; Li, Zhengtu; Huang, Wanyi; Guan, Wenda; Ma, Hongxia; Yang, Zi feng; Wang, Xinhua
Title: Efficacy and safety of Chou-Ling-Dan granules in the treatment of seasonal influenza via combining Western and traditional Chinese medicine: protocol for a multicentre, randomised controlled clinical trial
  • Document date: 2019_4_2
  • ID: vn9e5nm3_160
    Snippet: There is no connection between time and the test drug. Study flowchart. Participants that meet the inclusion criteria will be recruited and assigned randomly into three different groups. All participants will accept a 5-day treatment and 21-day follow-up period of observation. Data will be collected to evaluate the treatment efficacy and safety of Chou-Ling-Dan (CLD). 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 .....
    Document: There is no connection between time and the test drug. Study flowchart. Participants that meet the inclusion criteria will be recruited and assigned randomly into three different groups. All participants will accept a 5-day treatment and 21-day follow-up period of observation. Data will be collected to evaluate the treatment efficacy and safety of Chou-Ling-Dan (CLD). 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59

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