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Primary Cytoreductive Surgery With or Without Hyperthermic Intraperitoneal Chemotherapy (HIPEC) Summary View Full Description Full Description The objective of this study is to prove that treatment with primary cytoreductive surgery in combination with HIPEC (treatment arm) improves outcome compared to primary cytoreductive surgery without HIPEC (standard arm) with acceptable morbidity, in patients with FIGO stage III epithelial ovarian cancer who are eligible for primary cytoreductive surgery with no residual disease, or residual disease up to 2.5 mm.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria:
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There are 3 Locations for this study
City of Hope Duarte California, 91010, United States
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MSKCC New York New York New York, 10065, United States
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Rigshospitalet Copenhagen Copenhagen , , Denmark
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CHU de Besancon Besançon , , France
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Institut Bergonié Bordeaux , , France
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o Institut Bergonié, Bordeaux Bordeaux , , France
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Centre Leon Berard, Lyon Lyon , , France
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Institut du Cancer Montpellier Montpellier , , France
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Institut de Cancerologie de l'Ouest, ICO Nantes) Nantes , , France
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Institut Curie Paris Paris , , France
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CHRU Strasbourg Strasbourg , , France
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Oncopole, Institute Universitaire du Cancer de Toulouse (IUCT Toulouse) Toulouse , , France
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Mater Misericordiae University Hospital, Dublin Dublin , , Ireland
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Policlinico Sant'Orsola, Bologna Bologna , , Italy
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Fondazione Policlinico A Gemelli IRCCS Roma , , Italy
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Antoni van leeuwenhoek Amsterdam Noord-Holland, 1066C, Netherlands
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Amsterdam UMC
Catharina Hospital
Medisch Spectrum Twente
UMCG
Leiden University Medical Center (LUMC)
Maastricht UMC+
Radboud MC
Erasmus MC
Alice Bjoernlund-Larsen Uppsala , , Sweden
More Info How clear is this clinincal trial information?
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