ITMCTR2000004069尚未招募4 期
A randomized, double-blind, controlled, multicenter prospective clinical trial of Huoxiang Zhengqi Oral Liquid to prevent chemotherapy-induced nausea and vomiting following platinum-containing multi-day chemotherapy
West China Hospital, Sichuan University0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 年龄范围
- 18 至 70(—)
- 性别
- All
入选标准
- •1. Histologically or cytologically confirmed diagnosis of cancer;
- •2. Aged 18 to 70 years;
- •3. Accept chemotherapy for the first time and about to receive cisplatin (multi-day) highly emetogenic combination regimen or monotherapy regimen;
- •4. No history of chronic gastrointestinal diseases (such as chronic gastroenteritis, etc.), and no history of chronic nausea and vomiting (such as vertigo, Meniere disease, etc.);
- •5. Hematology, liver, kidney function, heart function and other important organ functions meet the requirements of chemotherapy.
排除标准
- •1. Have not yet controlled cancer pain, and need to titrate cancer pain or adjust the dose of opioid painkillers, or the digestive tract reaction of opioids has not been completely controlled;
- •2. Chronic receives corticosteroids;
- •3. Nausea and vomiting are caused for whatever reason in three days;
- •4. History of active gastrointestinal ulcer and gastrointestinal hemorrhage within one year;
- •5. Unable to read or understand the questionnaire or cannot complete the questionnaire independently;
- •6. Poor compliance and unable to complete the study as planned;
- •7. Cannot tolerate the smell of Huoxiang Zhengqi oral liquid or allergic to Huoxiang Zhengqi oral liquid;
- •8. Currently involved in any other clinical trial or observational study.
研究者
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