CTRI/2017/09/009920招募中未知
Modified Radical Neck Dissection versus Selective Neck Dissection for Node Positive Neck in Patients with Oral Squamous Cell Carcinoma : A Multicenter Prospective Randomised Controlled Trail
Head and Neck Coperative Oncology Froup0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
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
入选标准
- •1)The subject has a histologically confirmed squamous cell carcinoma of the oral cavity
- •2)The subjects age must be between 18 and 75 years
- •3)The subjects life expectancy is greater than 12 weeks and ECOG performance status 0 or 1
- •4)The subject has signed and dated the written informed consent
- •5)The subject is willing and able to fully participate for the duration of the study
- •6)If applicable, the subject has been counselled on tobacco cessation
- •7)Subjects are candidates for surgical intervention as determined by the anaesthesiologist of the institution at which he is undergoing treatment
排除标准
- •1)The subject has neck nodes on both sides of the neck, classified as N2c as per the AJCC Cancer Staging Manual 2010 OR neck nodes greater than 6cm in size, classified as N3 disease
- •2)The biopsy of the primary disease in the subject is a histology other than squamous cell carcinoma
- •3)The subject has a synchronous primary located in the upper aerodigestive tract or cancer of any other site
- •4)The subject has confirmed metastatic disease at initial clinical evaluation or during investigations
- •5)The subject is deemed not fit for surgeries due to medical conditions
- •6)The subject has received any previous surgery, radiotherapy or chemotherapy as treatment for his disease
- •7)The subject is not fit to receive radiation therapy due to personal choice, logistical reasons, or medical reasons
- •8)The subjects primary disease is localised to one side of the head and neck and is crossing the midline
- •9)The subject has nodal metastasis in levels IV or V
- •10) Subjects with pa st history of psychological illness seriously affecting the subjectâ??s ability to give an informed consent
- •11) The subject is, in the opinion of the Institutional Principal Investigator, not an appropriate candidate for study participation
- •12) The subject has participated in the study previously and was withdrawn
- •13) Screen Failure: All subjects considered for participation and found ineligible must be recorded in the Screen Failure Log. Subject confidentiality is maintained, but reason for exclusion is required.
- •14) The subject is part of another active clinical trial
研究者
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