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临床试验/JPRN-UMIN000000984
JPRN-UMIN000000984已完成3 期

A double-blind randomized controlled trial comparing 3mg and 1mg of ranisetron for the control of chemotherapy-induced acute emesis - Randomized controlled trial of granisetron for the prophylaxis of chemotherapy-induced emesis

Pharma Valley Center, Shizuoka Organization for Creation Industries0 个研究点目标入组 360 人开始时间: 2008年1月19日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
360

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)patients with history of hypersensitivity to 5-HT3 receptor antagonist and corticosteroids (2)patient who do not have enough whole body state to the antineoplastic agents treatment (3)pregnant or expecting woman (4)patient who enforces radiotherapy in the abdomen on the day of chemotherapy (5)uncontrollable diabetes mellitus (6)hepatitis B or C virus Carrier (7)patients having a clear vomiting symptom such as brain metastasis or obstruction to the passage of foods (8)the patient who judged inappropriate as an object of this study

研究者

发起方
Pharma Valley Center, Shizuoka Organization for Creation Industries

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