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Phase III clinical trial of bevacizumab with IV versus IP chemotherapy in ovarian, fallopian tube, and primary peritoneal carcinoma
eagle-i ID
http://hawaii.eagle-i.net/i/00000130-dd93-8f33-9953-50a980000000
Resource Type
Properties
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ClinicalTrials.gov url
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http://www.clinicaltrials.gov/ct2/show/NCT00951496?term=GOG-0252&rank=1
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Intervention
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Cisplatin
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Intervention
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Paclitaxel
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Intervention
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Carboplatin
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Additional Topic(s)
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Intraperitoneal infusion
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Additional Topic(s)
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Intravenous infusion
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Additional Topic(s)
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Progression-free survival
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Resource Description
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The purpose of this study is to determine if one or both of the proposed intraperitoneal chemotherapy regimens improves the progression-free survival (PFS) event rate compared to standard intravenous chemotherapy for first-line treatment of patients diagnosed with advanced stage ovarian, peritoneal or fallopian tube cancer. If both IP regimens significantly improve the PFS event rate compared to the standard regimen, then a second study objective is to determine whether IP cisplatin and IV paclitaxel on day one plus IP paclitaxel on day eight improves the PFS event rate when compared to the IP carboplatin and IV paclitaxel.
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Contact
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Berenberg, Jeffrey
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PI
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Berenberg, Jeffrey
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Topic
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peritoneal carcinoma
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Topic
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fallopian tube cancer
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Topic
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ovarian cancer
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Study Population
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Females aged 18 and older with histologically confirmed ovarian epithelial, fallopian tube, or primary peritoneal carcinoma.
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Website(s)
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http://www.cancer.gov/clinicaltrials/search/view?cdrid=650601&version=healthprofessional
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Funded by
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Gynecologic Oncology Group
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Phase
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Phase 3 clinical trial
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Performed by
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Clinical Protocol & Data Management Shared Resource
