JPRN-jRCTs051230110招募中2 期
An exploratory clinical study to evaluate the safety and short-term nutritional outcomes of postoperative enteral nutrition with a digestive-form nutrient in patients with esophageal cancer undergoing minimally invasive esophagectomy.
Goto Hironobu0 个研究点目标入组 32 人开始时间: 2023年10月10日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 32
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
- >= 18age old 至 ot applicable(—)
- 性别
- All
入选标准
- •(1) Age 18 years or older at the time of consent
- •(2) Diagnosed as cStage I/II/III (12th edition of the Esophageal Cancer Treatment Protocol) and underwent subtotal esophagectomy, primary reconstruction, enteral tube placement
- •(3) ECOG-PS 0-2
- •(4) Able to take oral intake before surgery
- •(5) Expected to undergo surgery within 60 days of study enrollment (within 60 days of completion of chemotherapy for patients undergoing preoperative chemotherapy)
- •(6) Patients are expected to be able to take oral intake for 3 months after surgery
- •(7) The patient's free written consent to participate in the study has been obtained.
排除标准
- •(1) The subject is allergic to oral nutritional supplements.
- •(2)Identified as allergic to any of the ingredients (especially soy and gelatin) in the test nutritional product, Hinex E-Gel LC.
- •(3) The subject has difficulty obtaining consent due to dementia or mental illness requiring treatment.
- •(4) The patient is taking steroids or immunosuppressive drugs due to an autoimmune disease, etc.
- •(5) Complicated viral infection requiring treatment.
- •(6) Other conditions deemed inappropriate by the Principal Investigator or Principal Investigators.
研究者
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