NCT02953769终止不适用
Use of Prevena Incision Management System in Wound Morbidity in Complex Ventral Hernia Patients. A Prospective Randomized Control Trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- AdventHealth
- 入组人数
- 61
- 试验地点
- 1
- 主要终点
- Primary Objective for Wound Care Comparison
研究概览
简要总结
Comparison of ventral hernia repair using standard wound care versus Prevena.
详细描述
Compare the outcomes for patients who have abdominal reconstruction for ventral hernia repair, regarding wound morbidity, post-operative pain and patient comfort to ambulation, with the use of Prevena™ to those patients who have ventral hernia repair to those who have standard wound care.
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 89 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 18 - 89
- •Open ventral hernia repair with or abdominal wall reconstruction after midline or non-midline defects.
- •Able to provide informed consent
排除标准
- •Immunosuppresses patients
- •Children 0 - 17
结局指标
主要结局
Primary Objective for Wound Care Comparison
时间窗: December 31, 2017
To quantify differences in the routine care of wound morbidity versus the use of Prevena™ by observing the healing process and obtaining quality of life by using the Carolinas Comfort Scale.
次要结局
未报告次要终点
研究者
研究点 (1)
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