NL-OMON49831已完成不适用
Detection of pituitary neuroendocrine tumor (PitNET) tissue during endoscopic transsphenoidal surgery using Bevacizumab-800CW: a single center feasibility and dose finding study - DEPARTURE
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 15
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
- •- Age >= 18 years
- •- Patients with an established diagnosis of PitNET with a Knosp grade of 3 or 4
- •who are scheduled to undergo TSS.
- •- WHO performance status 0-2
- •- Signed written informed consent
排除标准
- •- Medical or psychiatric conditions that compromise the patient's ability to
- •give informed consent
- •- Pregnant or lactating women. Documentation of a negative pregnancy test must
- •be available for woman of childbearing potential. Woman of childbearing
- •potential are pre- menopausal women with intact reproductive organs and women
- •less than two years after menopause
- •- History of infusion reactions to bevacizumab or other monoclonal antibody
- •- Inadequately controlled hypertension with or without current antihypertensive
- •medications
- •- Within 6 months prior to inclusion: myocardial infarction, TIA, CVA,
- •pulmonary embolism, uncontrolled chronic hepatic failure, unstable angina
研究者
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