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临床试验/JPRN-UMIN000009403
JPRN-UMIN000009403已完成3 期

A randomized, multicenter non-inferiority trial of 1-day versus 3-day dexamethasone in combination with palonosetron for prevention of nausea and vomiting induced by moderately emetogenic chemotherapy - A randomized, multicenter non-inferiority trial of 1-day versus 3-day dexamethasone in combination with palonosetron for prevention of nausea and vomiting induced by moderately emetogenic chemotherapy

Hokkaido University Hospital0 个研究点目标入组 300 人开始时间: 2012年11月27日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Serious or uncontrolled complication 2)Symptomatic or clinically suspected bone metastasis 3)Convulsive disorder needs anti-convulsant 4)Ascites fluid or pleural effusion needs paracentesis 5)Gastrointestinal obstruction 6)Vomiting and/or grade 2 or more nausea before chemotherapy 7)Hypersensitivity for 5-HT3 receptor antagonist 8)Hypersensitivity for dexamethasone 9)Pregnancy, lactation or who does not wish to contraception 10)History of palonosetorn administration 11)Capability or intention of cooperating 12)Participant in other anti-emetic trial 13)Undersirable for the patient to enter the trial

研究者

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