跳至主要内容
临床试验/JPRN-UMIN000005391
JPRN-UMIN000005391已完成2 期

Bevacizumab treatment of intra-venous administration and diagnostic nuclear medicine for symptomatic radiation necrosis in the brain - Bevacizumab treatment for symptomatic radiation necrosis

Department of Neurosurgery, Osaka Medical College0 个研究点目标入组 40 人开始时间: 2011年4月7日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
40

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
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients are able to undertake necrotomy; Intracranial tumors are active and recurrent (L/N ratio on F-BPA-PET is greater than 2.5, or L/N ration on C-MET-PET is greater than 1.8; Patients require intravenous administration of antibiotics, antiviral drugs, and antifugal drugs for infection; Febrile patients more than 38 degree Celsius of body temperature or equal; Patients having severe comorbidities such as heart diseases, pulmonary fibrosis, interstitial pneumonia, hemorrhagic diathesis, uncontrollable hypertension or diabetes; *Comorbidity or history of unstable angina and myocardiac infarction within 6 months *Uncontrollable peptic ulcer *Uncontrollable hypertension *Unhealed advanced wound or fracture *Comorbidity or history of gastrointestinal perforation and fistula, and abdominal abscess within 6 months *Comorbidity or history of emoptysis and pulmonary hemorrhage greater than Grade 1 *Comorbidity or history of vascular diseases (venous and arterial thrombosis and embolism, aortic aneurysms) required interventions within 6 months *Congestive heart failure more than NYHA class I *Patients with a schedule of an operation during this study or patients having had an operation within 4 weeks; Patients with hemorrhage (intracranial hemorrhage, gastrointestinal hemorrhage, urinary hemorrhage, hemoptysis); PT-INR is greater than 2.5 or unstable when warfarinization; History of severe hypersensitivity or allergy to bevacizumab; Pregnant patients, patients with a possibility of pregnancy, or patients breastfeeding; Investigators judge patients who are inappropriate to include this study.

研究者

发起方
Department of Neurosurgery, Osaka Medical College

相似试验