NCT01107314已完成不适用
Vasopressin Deficiency in Hemorrhagic Shock
The University of Texas Health Science Center at San Antonio1 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2010年2月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 81
- 试验地点
- 1
研究概览
简要总结
In this study we hope to delineate the typical vasoactive mediator response of trauma patients to shock. We plan to assess serum levels of vasopressin and also catecholamines, angiotensin, and cortisol during resuscitation of trauma patients to delineate high risk populations for vasopressin deficiency.
详细描述
This is a prospective observational study. The only research-driven procedure will be the removal of blood samples at designated time points(total blood removed 48 cc per patient). Hemodynamic, fluid infusion and agitation/pain data (RAMSEY Score) will prospectively be collected for research purposes. We will collect data from a convenience sample of patients (when research staff is available) over a one year period.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 98 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient is a male or female patient presumed to be at least 18 years of age;
- •Patient has a reported or actual systolic blood pressure < 90 mmHg within 1 hour of arrival to the Emergency Room;
- •Patient has clinical evidence of acute traumatic injury;
排除标准
- •Patient is asystolic or requires CPR prior to arrival;
- •Patient was transferred from an outside facility
- •Patient known to be pregnant
- •Patient known to be prisoner
研究者
研究点 (1)
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