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临床试验/ITMCTR2200005974
ITMCTR2200005974尚未招募1 期

Clinical intervention study of Chinese and Western medicine in people with AIDS immunocompromised state

Hubei Provincial Hospital of Traditional Chinese Medicine0 个研究点开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
尚未招募

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 65(—)
性别
All

入选标准

  • ? HIV antibody positive, confirmed by Western Blot confirmation test;
  • ? Voluntary acceptance of HAART;
  • ? CD4+ cell count <350 cells/µL;
  • ? The subjects are between 18-65 years old, male or female;
  • ? TCM syndrome differentiation is in line with lung-spleen deficiency syndrome or liver-kidney essence deficiency syndrome;
  • ? Voluntarily participate in this study, sign the informed consent form, and follow up on time.

排除标准

  • ? Those with uncontrolled serious opportunistic infections (Pneumocystis pneumonia, meningitis, esophageal Candida infection, lymphoma, Toxoplasma encephalopathy, tuberculosis, etc.) before enrollment;
  • ? Patients who are participating in clinical trials of other drugs within 1 month before enrollment;
  • ? Those who received immunomodulatory therapy within 1 month before enrollment;
  • ? White blood cell (WBC) count <2.0×109/L, or neutrophil (N) count <1.0×109/L, or hemoglobin (Hb) amount <90g/L, or platelet (PLT) count <75×109 /L, or liver or renal insufficiency (aspartate aminotransferase (AST), aspartate aminotransferase (ALT), total bilirubin (TBIL) = 2 times the upper limit of the reference value or urea nitrogen (BUN) ), serum creatinine (Scr) detection value = 1.2 times the upper limit of the reference value);
  • ? Patients with pancreatitis and active gastric ulcer;
  • ? Patients with clinically significant active diseases of the respiratory system, digestive system, circulatory system, blood system, neuroendocrine system, and urogenital system;
  • ? Those who suffer from autoimmune diseases;
  • ? Tumor patients who need chemotherapy;
  • ? Pregnant or breastfeeding women and women of childbearing age who do not use safe contraception;
  • ? allergic constitution;
  • ? Patients with intellectual or language barriers who cannot fully understand the test content or give good cooperation;
  • ? Other circumstances that the investigator considers inappropriate to participate in the trial.

研究者

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