JPRN-jRCTs051200009招募中未知
A randomized controlled trial of Ninjin yoeito in the perioperative period of lung cancer
Tanaka Yugo0 个研究点目标入组 140 人开始时间: 2020年5月1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
- 140
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
- >= 20age old 至 ot applicable(—)
- 性别
- All
入选标准
- •1. Patients over 20 years old with performance status of 0-1 who were diagnosed or suspected with primary lung cancer.
- •2. Patients undergoing uni-lobectomy with group-2 lymphadenectomy.
- •3. Patients who consented to the study in writing.
- •4. Patients scheduled to undergo thoracoscopic surgery including robot-assisted surgery.
排除标准
- •1. Patients who have history of allergies in NINJIN-YOUEI-TO in the past.
- •2. Patients who were treated with Kampo formulation for this symptom within 2 weeks before the start of this study.
- •3. Patients who have severe anorexia, nausea and vomiting which are careful administration of this drug.
- •4. Patients whom the doctor judged unsuitable as the subject.
- •5. Patients who do not retain liver function and kidney function
- •-Total Bilirubin <=2.0mg/dL
- •-Serum creatinine <=2.0mg/dL
- •6. Patients with conversion to open thoracotomy.
- •7. Patients with pulmonary resection range of 2 or more lobes.
- •8. Patients who cannot drink water within 3 days after surgery.
研究者
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