NCT07645547尚未招募不适用
Implementation of Prophylactic Negative Pressure Wound Therapy (ciNPWT) in High-Risk Patients in Gynecologic Oncology: A Prospective Feasibility Study and Nested Qualitative Analysis
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 30
研究概览
简要总结
This is a prospective, open-label, non-randomized interventional feasibility study with a nested qualitative analysis. The study exploratively verifies the feasibility of targeted prophylactic closed incision negative pressure wound therapy (ciNPWT) in clinical practice for patients with a high predicted risk of wound healing complications and compares the 30-day incidence of postoperative complications with standard dressing.
Participants will:
- Get ciNPWT or standard dressing after planned laparotomy
- Answer the questionairs about qualite of life
- Will visit the clinic 30 days after surgery to see the final result
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Adult female patients scheduled for planned abdominal surgery for gynecologic or gynecologic-oncologic indications.
- •Identification as "high-risk" for wound healing complications based on a clinical risk screening at admission.
- •Signed informed consent.
排除标准
- •Failure to provide informed consent.
研究者
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