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临床试验/ITMCTR2100004746
ITMCTR2100004746尚未招募1 期

The study of intraperitoneal hyperthermic perfusion chemotherapy combined with traditional Chinese medicine on survival status after laparoscopic ovarian cancer reduction surgery

Chengdu Women's and Children's Central Hospital0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
1 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
30 至 70(—)
性别
Female

入选标准

  • 1) Initial treatment of ovarian cancer (including rare types of ovarian tumors);
  • 2) Used for neoadjuvant chemotherapy and second HIPEC after intermittent cytoreductive surgery.
  • 3) Patients with epithelial ovarian cancer diagnosed by postoperative histopathology;
  • 4) Estimated survival time >= 6 months;
  • 5) Informed consent of the patient and family members, and signed informed consent form for hyperthermic perfusion.

排除标准

  • 1) Intestinal obstruction, extensive adhesions in the peritoneal cavity, and obvious inflammation in the abdominal cavity;
  • 2) There may be a high risk of poor postoperative anastomotic healing;
  • Factors, including anastomotic tissue edema, ischemia, obvious tension, severe hypoproteinemia, etc.;
  • 3) Major organ dysfunction such as heart, kidney, liver, and brain;
  • 4) Severe coagulation dysfunction; bile obstruction and ureteral obstruction;
  • 5) Aged >= 75 years old is a relative contraindication.

研究者

发起方
Chengdu Women's and Children's Central Hospital

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