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Clinical Trial Summary

The combination of paclitaxel and carboplatin is the standard first-line chemotherapy for ovarian cancer as recommended by the NCCN Guidelines for Epithelial Ovarian Cancer, and is conventionally given via intravenous route every three weeks. The addition of target therapy (bevacizumab) has shown to improve progression free survival but not overall survival. Several trials have also demonstrated a clinically significant survival advantage associated with intraperitoneal chemotherapy compared to intravenous chemotherapy, and the best outcomes are consistently seen for patients who have no residual disease. This study aims to compare triweekly chemotherapy with bevacizumab versus intraperitoneal chemotherapy in patients with advanced stage ovarian cancer.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT05410938
Study type Observational
Source Far Eastern Memorial Hospital
Contact
Status Completed
Phase
Start date June 6, 2022
Completion date May 1, 2023