NCT02368730已完成不适用
Documentation of the Efficacy of Desmopressin (MINIRIN Parenteral 4 Microgram/ml Solution for Injection) Within the Context of Surgical Procedures
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 23
- 试验地点
- 1
- 主要终点
- Change in platelet function pre- and post-administration of desmopressin
研究概览
简要总结
In this non-interventional multicentre, prospective, observational cohort study, the efficacy of desmopressin is evaluated in patients with platelet dysfunction due to acetylsalicylic acid or cox-1-inhibitors within the context of surgical procedures.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Pre-, peri- or postoperative treatment with a standard dose of desmopressin as a result of platelet dysfunction (disturbance of blood platelet function) due to treatment with acetylsalicylic acid or cox-1-inhibitor.
- •Decision on the therapy with MINIRIN parenteral 4 Microgram/ml solution for injection has already been made independently by the physician beforehand
- •The patients (≥ 18 years) have been informed about the non-interventional study and have given their written consent for participation
排除标准
- •Participation in a clinical trial
- •Treatment with acetylsalicylic acid for cardiovascular indications
研究组 & 干预措施
desmopressin
Treatment according to standard clinical practice.
干预措施: desmopressin (Drug)
结局指标
主要结局
Change in platelet function pre- and post-administration of desmopressin
时间窗: From baseline up to 7 days
As measured by Platelet Function Analyzer (PFA) 100/200
次要结局
未报告次要终点
研究者
研究点 (1)
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