NCT05964166已完成不适用
Tetragraph® Monitor: Tolerance of Preoperative Placement
Joseph D. Tobias1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年5月31日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Tolerance to Preop Placement as Assessed by Likert Scale
研究概览
简要总结
This is a prospective, non-blinded, single arm study. The primary objective of this study is to evaluate the tolerance to preoperative placement of the adhesive sensor for the Tetragraph® Neuromuscular Transmission Monitor in pediatric-sized patients ≤ 12 years of age.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 3 Months 至 12 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients requiring anesthetic care and use of neuromuscular blockade
- •Age ≤ 12 years
排除标准
- •History of a peripheral neurologic or neuropathic disorder
- •Upper extremity cannot be used for TOF monitoring
- •Undergoing a surgical procedure in which neuromuscular blockade is not required
- •Patient is edematous
- •Patients with significant behavioral or neurocognitive issues which affect behavior and impact the ability to place the sensor
研究组 & 干预措施
Tetragraph
Experimental
干预措施: TetraGraph NMT Monitor (Device)
结局指标
主要结局
Tolerance to Preop Placement as Assessed by Likert Scale
时间窗: 30 mins. prior to surgery
Patient's tolerance to preoperative placement of the adhesive sensor for the Tetragraph® Neuromuscular Transmission Monitor will be assessed by using a 10-point Likert scale with 0=very badly/pulled sensor off and 10=very well/left sensor alone.
次要结局
- Application Ease(30 minutes prior to surgery)
研究者
Joseph D. Tobias
Chief of Anesthesiology & Pain Medicine
Nationwide Children's Hospital
研究点 (1)
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