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临床试验/ITMCTR2200005920
ITMCTR2200005920招募中4 期

Efficacy and safety evaluation of Tanreqing Capsules in the treatment of community-acquired pneumonia (phlegm-heat obstructing lung syndrome) in adult: A randomized, double-blind, placebo-controlled, single-c

The First Affiliated Hospital of Guangzhou University of Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
18 至 80(—)
性别
All

入选标准

  • All the following criteria must be conformed before inclusion:
  • ?Inpatient aged from 18 to 80;
  • ?Conforming diagnosis criteria of non-severe CAP;
  • ?Conforming TCM diagnosis criteria of wind-warmth and lung-heat disease, phlegm-heat obstructing lung syndrome;
  • ?Patients with clear consciousness, articulateness and adequate understanding of the trail process;
  • ?Volunteer to participate in clinical trial with favorable compliance and signed informed consent.

排除标准

  • Conforming to any term of the following criteria must be excluded:
  • ?Patients with severe CAP
  • ?Women who are pregnant or breastfeeding
  • ?Patients with TRQC-relative allergic history or ADR history
  • ?Patients with lung cancer, pulmonary tuberculosis, pulmonary atelectasis or pulmonary edema, etc.;
  • ?Patients with psychiatric disorder or severe primary diseases of the cardio-cerebrovascular, liver, kidney or hematopoietic system;
  • ?Patients with chronic alcohol or drug abuse;
  • ?Patients who are participating in other clinical trials or have participated in other clinical trials within 1 month;
  • ?Patients with viral, mycoplasma or chlamydia infection suggested by pathogenetic examination.

研究者

发起方
The First Affiliated Hospital of Guangzhou University of Chinese Medicine

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