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临床试验/NCT01893463
NCT01893463撤回不适用

Prospective Study to Evaluate the Safety and Effectiveness of the iTClamp50 to Provide Temporary Wound Closure

Innovative Trauma Care Inc.1 个研究点 分布在 1 个国家开始时间: 2013年8月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
试验地点
1
主要终点
Number of Adverse Events

研究概览

简要总结

Early and effective control of severe bleeding is critical to survival of trauma patients. The iTClamp™50 is a Health Canada approved medical device for temporary wound/skin closure that quickly controls bleeding by sealing the skin. Similar to a clip, the device seals the skin edges within a pressure bar, enabling the creation of a hematoma where blood collects under pressure to form a stable clot until definitive repair. The iTClamp50 is indicated for use as a skin closure device for short-term soft tissue approximation, including use in trauma wounds, lacerations, junctional bleeds or surgical incisions. The purpose of this prospective clinical study is to evaluate the effectiveness and safety of the iTClamp50 in the ambulance (pre-hospital) and emergency department setting. This will be accomplished by observing patients with the device applied from the pre-hospital through to patient discharge. The hypothesis is that the iTClamp50 will be safe and effective at providing temporary wound closure to control hemorrhage in the pre-hospital and emergency department setting.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • The device is indicated for use to control external hemorrhage from all compressible areas and to close wounds on the torso (chest and abdomen). The final decision to apply the device will be left with the care provider; however, their rationale will be reviewed in the post-use questionnaire.

排除标准

  • The device is contraindicated for application to specific regions (e.g., eyes and genitals), application on patients less than the size of maturity, and wounds in which the skin edges cannot be approximated.

结局指标

主要结局

Number of Adverse Events

时间窗: Until patient discharge

Effectiveness of the iTClamp50 to control hemorrhage

时间窗: Patient discharge (Varies)

As measured by length of time to control bleeding and evidence of re-bleeding

次要结局

  • Pain associated with application and removal of the iTClamp50(Patient discharge (varies))

研究者

发起方
Innovative Trauma Care Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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