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Delayed Nausea and Vomiting in Patients With Colorectal Cancer Receiving Oxaliplatin Summary RATIONALE: Learning how often patients experience nausea and vomiting after receiving anti-vomiting medicine and chemotherapy for colorectal cancer may help doctors plan better treatment and improve patients' quality of life. PURPOSE: This clinical trial is studying delayed nausea and vomiting in patients with colorectal cancer receiving standard anti-vomiting medicine during the first course of chemotherapy.
View Full Description Full Description OBJECTIVES: To assess the prevalence of delayed nausea and vomiting in patients with colorectal cancer receiving standard anti-emetic medications during the first course of an oxaliplatin-based chemotherapy regimen (mFOLFOX6 or FOLFOX7). OUTLINE: This is a multicenter study. Patients undergo collection of demographic, diagnostic, and treatment data at baseline. Patients complete the Functional Living Index-Emesis (FLIE) questionnaire at baseline prior to first chemotherapy infusion and at 5-7 days. Patients also fill out daily patient diaries about symptoms of nausea and vomiting, and use of medications to prevent these symptoms over days 1-5.
View Eligibility Criteria Eligibility Criteria DISEASE CHARACTERISTICS: Diagnosis of colorectal cancer Currently receiving OR scheduled to receive the first course of either of the following chemotherapy regimens: mFOLFOX6 FOLFOX7 No clinical or imaging evidence of brain metastasis PATIENT CHARACTERISTICS: Able to maintain a diary and complete a standardized quality of life questionnaire in English PRIOR CONCURRENT THERAPY: See Disease Characteristics More than 90 days since prior aprepitant
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There is 1 Location for this study
Beth Israel Medical Center - Philipps Ambulatory Care Center New York New York, 10003, United States
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