IRCT20191103045317N1已完成3 期
Comparison between the effect of Triplet Aprepitant/Dexamethasone/Ondansetron vs. doublet Dexamethasone/Ondansetron for prevention of moderately emetogenic chemotherapy: placebo-controlled double blind, randomised clinical trial of efficacy
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 90
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
- 18 years 至 70 years(—)
- 性别
- All
入选标准
- •Cancer patients receiving moderate emetogenic chemotherapy regimens,formed the study cohort.
- •Eligible patients were adults (aged between 18 - 70 years) with a karnofsky index of 50% or more).
- •Women at reproductive ages should had undertaken an appropriate contraceptive method
排除标准
- •causes of nausea or vomiting unrelated to the chemotherapy (e.g., gastrointestinal obstruction, massive ascites, widespread brain metastases, history of motion sickness or vestibular dysfunction, uremia or electrolyte disturbance)
- •active infection
- •uncontrolled seizure
- •candidate for radiation therapy of brain or upper abdomen in less than a week
- •an emetic episode 24 h before initiation of chemotherapy
- •complications that prohibited Dexamethasone use
- •one of the followings observed in their lab studies : wbc<3000/mm3 , anc<1500/m m3 , plt<100000 mm3, ALT & AST>2.5 * upper limit of normal,Bill & Cr > 1.5* upper limit of normal
- •opium addicted
- •poor compliance
- •receiving corticosteroids for more than 3 months and more than 50 mg Prednisone daily;
- •Carlson’s comorbidity scale of 3 or more
- •Any drugs with antiemetic efficacy other than the study drugs wouldn’t been allowed before the study started, and were recorded on.
研究者
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