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临床试验/NL-OMON53297
NL-OMON53297尚未招募2 期

A phase 2 intervention study: Detection of early esophageal neopastic lesions by quantified fluorescence molecular endoscopy using oral and topical administration of bevacizumab-800CW and cetuximab-800CW - Oral fluorescent tracer administration to detect esophageal adenocarcinoma

niversitair Medisch Centrum Groningen0 个研究点目标入组 25 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
入组人数
25

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
18 至 99(—)

入选标准

  • - BE patients without dysplasia and with suspected/diagnosed LGD, HGD or
  • superficial EAC and planned diagnostic and/or therapeutic endoscopy
  • - Written informed consent is obtained

排除标准

  • - Patients under the age of eighteen.
  • - Submucosal and invasive EAC, also defined as EAC with TNM-classification
  • other than T1.
  • - Previous radiation therapy for esophageal cancer
  • - Known immunoglobulin allergy
  • - Previous chemotherapy, immunotherapy or related surgery
  • - Prior bevacizumab or cetuximab treatment
  • - Medical or psychiatric conditions that compromise the patient*s ability to
  • give informed consent
  • - Pregnancy or breast feeding.

研究者

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