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临床试验/NCT07256951
NCT07256951招募中不适用

Gen 2 Battrode Wear Study

Baxter Healthcare Corporation2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年11月12日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
2
主要终点
Wear time

研究概览

简要总结

Validating adhesive wear time

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Device Feasibility
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participant is ≥ 18 years.
  • Completes the consent process as required.
  • Participants can speak and read English fluently.
  • Willing to allow shaving of device application area, as required.
  • Willing to take photos of the application area before wear, daily during wear, and immediately after removal.
  • Willingness to report current known pregnancy.

排除标准

  • Unable to comply with the study protocol and instructions for wearing the devices for up to 15 days.
  • Any pre-existing breached or compromised skin, skin rash, irritation or infection at the application area.
  • Any incision, wound or scar in the application area.
  • Participants with known skin allergies and sensitivities to adhesives.
  • Participants with scheduled electronic imaging (including magnetic resonance imaging), cardioversion, and/or procedures where device would be removed during the data collection period.
  • Participants with known history of cardiac arrhythmias.
  • Participants with chest anatomies not compatible with secure parasternal placement.
  • Use of clothing or garment that can dislodge or loosen the patch or bras with underwires or other worn items that might interfere with the devices under study.

结局指标

主要结局

Wear time

时间窗: 15 days

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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