This is a phase III, multicenter, interventional and randomized study which evaluates the use of Hyperthermic Intraperitoneal Chemotherapy (HIPEC) coupled with either Primary Debulking Surgery (PDS) or Interval Debulking Surgery (IDS), in patients with ovarian cancer. This study aims to assess the efficacy, in terms of disease-free survival (DFS), the use of HIPEC combined with standard care (PDS or IDS) or standard care alone.
The primary objective of this study is to assess the efficacy, in terms of disease-free survival (DFS), the use of HIPEC treatment combined with standard care (PDS or IDS) or standard care alone (PDS or IDS alone).
Secondary objectives of the study include:
Exploratory objectives (optional) include:
Condition | Ovary Neoplasms, Ovarian Cancer, Ovarian Carcinoma |
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Treatment | HIPEC |
Clinical Study Identifier | NCT03842982 |
Sponsor | Centre Oscar Lambret |
Last Modified on | 7 February 2022 |
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