The purpose of this clinical trial is to Investigate whether the administration of HIPEC with Cisplatin (75 milligrams per square meter of body surface) after surgical cytoreduction in women with ovarian, tubal or primary peritoneal carcinoma increased disease-free survival period compared with patients without HIPEC treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
32
Cytoreduction
Intraoperative Intraperitoneal Hyperthermic Chemotherapy (Hipec)+Cisplatin
Hospital Clínico Universitario Virgen de la Arrixaca
El Palmar, Murcia, Spain
RECRUITINGdisease-free survival period
Every three months until recurrence of disease.
Time frame: Every 3 months up to 30 months
Evaluation of overall survival.
Every three months until recurrence of disease.
Time frame: Every 3 months up to 30 months
Study of morbidity.
Every three months until recurrence of disease.
Time frame: Every 3 months up to 30 months
Evaluation of quality of life related to the procedure.
Every three months until recurrence of disease.
Time frame: Every 3 months up to 30 months
Study of Ex vivo correlation.
in vitro cell culture to study the effect of temperature and cisplatin on cell viability
Time frame: 4 days post surgery
Pedro Cascales Campos, MD,PhD
CONTACT
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