临床试验/NCT00792597

NCT00792597已完成不适用

Comparison of Three Methods of Hemoglobin Monitoring in Patients Undergoing Spine Revision or Hip Revision Surgery.

University of California, San Francisco1 个研究点分布在 1 个国家目标入组 20 人开始时间: 2009年4月最近更新: 2013年3月7日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方: University of California, San Francisco
入组人数: 20
试验地点: 1
主要终点: See description below

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to compare the hemoglobin results obtained with 1) the HemoCue™, 2) the Masimo SpHb™, and 3) the UCSF Clinical Laboratory. The goal is to determine if these three values differ from each other during various levels of blood loss in the clinical care of patients for spine revision and hip revision surgery.

详细描述

See above

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

•Male or non-pregnant female 18 y/o or older
•American Society of Anesthesiology Classification 1, 2 or 3
•Scheduled to undergo spine or hip revision surgery

排除标准

•Pregnant or nursing
•Patients who in the study investigators clinical judgement would not be suitable for research.

结局指标

主要结局

See description below

时间窗: A minimum of three differences recorded during surgery

Primary outcome is based on the difference between SpHb (Masimo SpHb™ continuous hemoglobin reading ) - tHb (laboratory hemoglobin determination).

次要结局

See description below(A minimum of three differences recorded during surgery)

研究者

发起方

University of California, San Francisco

申办方类型

Other

责任方

Sponsor

研究点 (1)

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