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临床试验/JPRN-jRCTs051200009
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

发起方
Tanaka Yugo

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