跳至主要内容
临床试验/NL-OMON49831
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

niversitair Medisch Centrum Groningen0 个研究点目标入组 15 人开始时间: 待定最近更新:
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

相似试验