NL-OMON45310撤回不适用
Deferoxamine in Aneurysmal Subarachnoid Hemorrhage trial - DASH
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 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
- 18 至 64（—）
入选标准
- •* Male or Female,
- •* 18-85 years old inclusive,
- •* subarachnoid hemorrhage diagnosed by CT on admission,
- •* Randomizable within 72 hours of subarachnoid hemorrhage,
- •* Saccular intracranial aneurysm proven by cerebral angiography or CTA,
- •* Surgical or endovascular obliteration is performed,
- •* Able to obtain written informed consent from patient or surrogate.
- •* Patients in good clinical grade (WFNS 1-3)
排除标准
- •* Pregnancy, as confirmed by routine urine test on admission,
- •* Abnormal renal function at time of randomization (GFR <60 mL/min)
- •* Elevated liver function test at time of randomization (AST > 45 U/L and ALT > 35 U/L.)
- •* History of liver disease or active liver disease, Active renal disease,
- •* Hypersensitivity to deferoxamine,
- •* Patient taking medication not recommended for concomitant use with deferoxamine as per the product label (e.g. high dose vit. C medication).
- •* Patients not able to complete the study follow-up.
研究者
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