临床试验/CTIS2023-506395-27-00

CTIS2023-506395-27-00招募中1 期

DETOUR; Determining the safety and feasibility of optical coherencetomography and near infrared fluorescence: a prospective pilotintervention study

niversitair Medisch Centrum Groningen0 个研究点目标入组 15 人开始时间: 2023年10月2日最近更新: 2024年7月22日

适应症

试验速览

阶段: 1 期
状态: 招募中
发起方: niversitair Medisch Centrum Groningen
入组人数: 15

研究概览入排标准研究者记录与标识符相似试验

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 65+（—）
性别: All

入选标准

•Indication for a therapeutic endoscopy procedure (EMR or ESD), Age = 18, Written informed consent

排除标准

•Submucosal and invasive EAC or CRC, Radiation therapy for esophageal or colorectal cancer, History of infusion reactions to Bevacizumab or other monoclonal antibodies, Chemotherapy, immunotherapy or surgery 28 days before administration of the tracer, Non-adjustable hypertension, Medical or psychiatric conditions that compromise the patient’s ability to give informed consent, Pregnancy or breast feeding; a negative pregnancy test must be available for women of childbearing potential

研究者

发起方

niversitair Medisch Centrum Groningen

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