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临床试验/ITMCTR1900002399
ITMCTR1900002399尚未招募4 期

Clinical efficacy of arsenic trioxide combined with carboplatin for neoadjuvant chemotherapy for locally advanced cervical cancer

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
尚未招募
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
20 至 60(—)
性别
Female

入选标准

  • 1 Aged 20-60 years;
  • 2 Patients with stage IB2, IIA2, IIB cervical cancer;
  • 3 Normal blood analysis, liver and kidney function before treatment;
  • 4 No evidence of distant metastasis;
  • 5 No serious heart, liver, kidney and blood system and other important organ diseases;
  • 6 Patients have signed the informed consent

排除标准

  • 1 Early or small lesions do not require neoadjuvant chemotherapy patients;
  • 2 cachexia:PS score = 3 points, KPS score < 70 points;
  • 3 Active infection or bleeding;
  • 4 Complete intestinal obstruction;
  • 5 Uncontrolled psychosis;
  • 6 Pregnant and lactating women;
  • 7 Allergic constitution, or known to arsenic allergy patients;
  • 8 Late no possibility of surgery patients;
  • 9 Patients who are unwilling to receive neoadjuvant chemotherapy combined with surgery in the advanced stage;
  • 10 Patients with severe comorbidities;
  • 11 Patients who cannot tolerate chemotherapy and surgical words; 13 Patients who have participated in other clinical trials in the last 3 months;
  • 12 Any other conditions that the investigator considers unsuitable for participation in this trial.

研究者

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

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