Prophylactic Negative Pressure Wound Therapy in Obese Women at Cesarean: a Multicenter Randomized Trial
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 1,624
- 试验地点
- 12
- 主要终点
- Number of Participants With Superficial or Deep Surgical Site Infections (SSIs)
研究概览
简要总结
The Prophylactic Negative Pressure Wound Therapy in Obese Women at Cesarean Trial is a large pragmatic multi-center randomized clinical trial designed to evaluate the effectiveness, safety and cost-effectiveness of prophylactic negative pressure wound therapy (NPWT) - a closed, sealed system that applies negative pressure to the wound surface via a single-use, battery-powered, portable device - to decrease surgical site infections (SSIs) in obese women.
详细描述
Experimental evidence suggests that NPWT promotes wound healing by removing exudate, approximating the wound edges, and reducing bacterial contamination. Obesity (body mass index [BMI] ≥30kg/m2) increases the risk for both cesarean delivery and SSIs compared to non-obese women. The increased risk of SSIs is in part due to the increased thickness of the subcutaneous space, allowing collection of exudates and increasing tension on wound edges, promoting the growth of bacteria, and leading to wound infection and breakdown. Thus, prophylactic NPWT may be particularly effective in this patient population.
During the 5-year project period, investigators from 4 collaborating perinatal centers in the United Stated (two university and two community) will randomize 2850 obese women undergoing cesarean delivery to receive either prophylactic negative pressure wound therapy with the Prevena device or standard wound dressing. Women will be followed up to 30 days postoperatively to ascertain study outcomes.
The primary outcome for the trial is superficial or deep SSI after cesarean according to the CDC's National Healthcare Safety Network definitions. The investigators will also assess other wound complications, adverse events potentially attributable to NPWT and cost-effectiveness as measured by incremental cost per case of SSI prevented and per quality-adjusted life year (QALY).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 16 Years 至 —(Child, Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- •Non-availability for postoperative follow-up
- •Contraindication to NPWT applicable to women undergoing cesarean: Pre-existing infection around incision site, Bleeding disorder, Therapeutic anticoagulation, Irradiated skin, Allergy to any component of the dressing (e.g. silver, acrylic, silicone, adhesive tape)
结局指标
主要结局
Number of Participants With Superficial or Deep Surgical Site Infections (SSIs)
时间窗: 30 days postoperatively
As defined according to the Center for Disease Control and Prevention's (CDC) National Healthcare Safety Network criteria.
次要结局
- Patient Satisfaction Score(At postoperative day 30)
- Number of Participants With Wound Hematoma, Seroma, Separation (Other Wound Complications)(30 days postoperatively)
- Number of Participants With a Composite of Any Wound Complication Including SSI, Hematoma, Seroma, Separation (2cm or More).(30 days postoperatively)
- Patient Pain Score(At postoperative day 30)
- Number of Participants With Skin Blistering, Erythema, Wound Bleeding (Measures of Adverse Skin Events)(30 days postoperatively)
- Number of Participants With Organ Space SSIs (Endometritis, Intraabdominal Abscess)(30 days postoperatively)
- Number of Participants With Superficial, Deep or Organ Space SSIs (Individual Types of SSIs)(30 days postoperatively)
- Number of Participants With Physician Office Visit, Emergency Room Visit, Attendance at Wound Clinic, Use Antibiotics, Hospital Readmission for Wound Related Problems (Measures of Healthcare Resource Utilization)(30 days postoperatively)
研究者
David Haas
Professor of Obstetrics and Gynecology
Indiana University
