JPRN-jRCT1031210136招募中未知
A randomized, open-label, parallel-group study of the efficacy of oral Ninjin'yoeito in improving fatigability and nutritional status in the perioperative period of primary lung cancer - Efficacy of oral Ninjin'yoeito for improvement of fatigability and nutritional status in the perioperative period of primary lung cancer
Ishibashi Hironori0 个研究点目标入组 332 人开始时间: 2021年6月9日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 332
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
- >= 65age old 至 ot applicable（—）
- 性别
- All
入选标准
- •1. Patients aged 65 years or older who will undergo anatomical lung resection and systematic lymph node dissection for primary lung cancer at our department.
- •2. Patients who have given written consent for this study.
- •3. Patients with primary lung cancer in stages 0, I, II and III.
排除标准
- •1. The patient does not give consent to participate in the study.
- •2.The patient has a history of allergy to Ninjin'yoeito or its components.
- •3. The patient has severe anorexia, nausea, or vomiting, which is a cautious administration of the study drug.
- •4. The patient with severe hepatic or renal dysfunction.
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