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Study identifier: NCT04282356 Synced from ClinicalTrials.gov · July 29, 2026
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Intensive Intraperitoneal Therapy in Advanced Ovarian Cancer

Condition: Ovarian Cancer · Intraperitoneal Chemotherapy  ·  Sponsor: Institut du Cancer de Montpellier - Val d'Aurelle

PhasePhase 2
Planned participants55
Who can joinFemale, 18 Years to 75 Years
Healthy volunteersNo

About this study

Clinicians postulate that it may be interesting to combine the two IntraPeritoneal (IP) treatments associated with a significant improvement of OC overall survival i.e. cytoreductive surgery with hyperthermic intraperitoneal chemotherapy (HIPEC) and postoperative intraperitoneal chemotherapy (IPC) as an " intensive peritoneal " regimen in the initial management of stages III-IVA ovarian cancers. Performing a postoperative IPC may allow completing and extending the duration of the effect of HIPEC in decreasing the risk of peritoneal recurrence. HIPEC may also allow administering an early IP treatment on the residual microscopic disease during initial or interval surgery with an optimal access to the intraperitoneal cavity. Postoperative IPC will extend the HIPEC effect on unsterilized peritoneal microscopic residues with the aim of decreasing the risk of local recurrence. Performing HIPEC before IPC could allow limiting the number of postoperative IP courses needed. Nevertheless, this association questions its feasibility and tolerance, which should both be assessed in a phase II trial. Clinicians propose to conduct this feasibility study combining for the first time HIPEC with IPC as first-line treatment of ovarian cancer with peritoneal carcinomatosis to perform a peritoneal intensification.

This description comes directly from the study's public registry record.

Talk to the study team

Aurore MOUSSION  ·  0467613102  ·  DRCI-icm105@icm.unicancer.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Institut du Cancer de Montpellier - Val d'AurelleMontpellier, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT04282356