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临床试验/JPRN-UMIN000032336
JPRN-UMIN000032336招募中未知

Assessment of the efficacy and safety of accessory nerve reconstruction using nerve regeneration inducing tube in neck dissection for patients with head and neck cancer - A Prospective Multicenter Clinical Study - Assessment of the efficacy and safety of accessory nerve reconstruction using nerve regeneration inducing tube in neck dissection- A Prospective Multicenter Clinical Study

Yokohama City University0 个研究点目标入组 12 人开始时间: 2018年4月20日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
12

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
20years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)Patients who underwent the ipsilateral neck dissection or radiotherapy before. 2)Patients who registered other clinical trial (intervention study or Japanese registration trial) for head and neck cancer before. 3)Patients with infections requiring systematic treatment 4)Multiple malignancies except for carcinoma in situ and intramucosal cancer. 5)uncontrolable diabetes 6)severe heart disease such as myocardial infarction within six months and unstable angina. 7)uncontrolabel hypertension 8)pulmonary disease with over class 3 in American Society of Anesthesiologists physical status classification 9)Patients with a history of hypersensitivity for polyglycolic acid and collagen. 10)Patients with continuous systemic administration of steroid or immunosuppressant 11)Patients with the possibility of pregnancy or pregnancy 12)Patients who are unable oral administration of mecobalamin 13)Patients with gastrointestinal disorders inhibiting the absorption of mecobalamin 14)Patients with mental illness, alcoholism,drug addiction affecting the compliance with the clinical trial. 15)Patients who are judged by an investigator to be inappropriate for this study for any other reason.

研究者

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