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Clinical Trial Summary

The primary objective is to estimate overall survival after secondary cytoreductive surgery and HIPEC for women with recurrent primary mucinous ovarian cancer


Clinical Trial Description

PRIMARY OBJECTIVE: The primary objective is to estimate progression-free survival (PFS) after secondary cytoreductive surgery and HIPEC for women with recurrent primary mucinous ovarian cancer SECONDARY OBJECTIVES: - To estimate overall survival (OS) after secondary cytoreductive surgery and HIPEC for women with recurrent primary mucinous ovarian cancer - To evaluate toxicity and morbidity of secondary cytoreductive surgery and HIPEC for women with recurrent primary mucinous ovarian cancer - To estimate quality of life after secondary cytoreductive surgery and HIPEC for women with recurrent primary mucinous ovarian cancer - To estimate what proportion of patients who preoperatively appear to be candidates for secondary cytoreductive surgery and HIPEC are found to have unresectable disease at time of surgical exploration - To collect blood and tumor samples for biobanking to be used for exploratory endpoints ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05123807
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Michael Frumovitz, MD
Phone 713-792-9599
Email [email protected]
Status Not yet recruiting
Phase Phase 2
Start date April 30, 2022
Completion date October 31, 2023

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