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

Phase 1
Conditions
Ovarian cancer
Registration Number
ITMCTR2100004746
Lead Sponsor
Chengdu Women's and Children's Central Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

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.

Exclusion Criteria

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.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Quality of Life;
Secondary Outcome Measures
NameTimeMethod
Imaging data;Tumor markers;Drug side effects;
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