Use of an Occlusive Skin Closure System May Reduce Post-operative Wound Drainage After Tumor Arthroplasty of the Hip
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 70
- 试验地点
- 2
- 主要终点
- Wound status
研究概览
简要总结
Study Type: Investigator initiated, non-significant risk
Study Objective(s): To establish the effect of occlusive wound closure with the DERMABONDTM PRINEO skin closure system, compared to routine wound closure with skin staples, on post-operative wound discharge (PWD) after tumor arthroplasty of the hip
Study Population: Patients with secondary tumors of bone, undergoing tumor resection and primary endoprosthetic reconstruction involving the hip joint
Inclusion Criteria:
- Bone resection and endoprosthetic reconstruction for metastatic bone lesions involving the proximal femur or acetabulum
- Imminent, or de-facto pathologic fractures of proximal femur and/or acetabulum, requiring endoprosthetic reconstruction (with or without bone resection) involving the hip joint
Exclusion Criteria:
- Minors
- Pregnant and breast-feeding women
- Skin defects and wound conditions not amenable to primary wound closure and other DERMABOND PRINEO contraindications
- Underlying infection
- Total femur replacements
- Implant revision procedures
Structure: Open 2-arm prospective randomized controlled trial.
Duration of Study: 18 -24 months Multi-center: No Masking/Blinding: No Method of Subject Assignment: Block Randomization (10 in each block) Concurrent Control: Active - wound closure with skin staples Estimated Total Sample Size: 70 subjects will be enrolled in this study Statistical Rationale Provided: Yes Statistical Methods: Student t test for unpaired data
Study Endpoints:
- Time to dry wound status (in post-operative days)
- Duration of antibiotic use (in post-operative days)
- Length of hospital stay (in post-operative days)
详细描述
Background:
Patients undergoing bone tumor resection and subsequent endoprosthetic reconstruction are at significant risk of developing prosthetic joint infection (PJI)Additionally, numerous factors contribute to a significant predisposition of these patients to wound healing complications, including the burden of their primary disease, associated comorbidities, previous or ongoing treatment often involving chemotherapy and or radiotherapy, and the extent of the necessary surgical procedure. In a retrospective review of this specific patient population treated at the investigators institution during recent years, the investigators have found a very high prevalence of persistent discharge from the surgical wound, when routine wound closure with skin staples was used. This is of particular concern, as an association of this post-operative complication with a higher incidence of PJI has been clearly established in several large studies on conventional total hip arthroplasty. Another previous study showed that prolonged wound discharge (PWD) will often lead to increased length of hospital stay and increased use of antibiotics to prevent infection. In the same study, the investigators were able to demonstrate a substantial reduction of PWD, use of intra-venous antibiotics and length of hospital stay, with use of an alternative skin closure method, combining intradermal suture and Steristrips for optimal wound edge apposition and a topical skin adhesive (2-octyl cyanoacrylate) as a sealant. However, more extensive data on the prevalence of persistent surgical wound discharge and the preventive effect of skin adhesives as an adjunct to wound closure in high-risk patient populations are lacking in the literature.
Investigational Product:
The DERMABOND PRINEO Skin Closure System has been specifically developed with the goal to achieve fast and secure closure of long incisions. It consists of two components, a pressure sensitive adhesive (PSA) initiated flexible mesh, designed for wound edge approximation and a cyanoacrylate based topical skin adhesive for occlusive wound closure. Intradermal suture is not necessary, as this system has been shown to support wound closure strength equivalent to subcuticular 3-0 sutures and is able to provide even distribution of tension across the entire incision length to ensure wound edge approximation throughout the wound healing process. Furthermore, compared to subcuticular suture, it has demonstrated equivalent wound healing and cosmesis at 90 days, while reducing wound closure time by up to 70%. It also provides an immediately effective occlusive barrier with documented antimicrobial properties, enabling patients to shower directly following a procedure and can be easily removed after the patient's natural wound healing process is complete, estimated at anywhere between 12 to 25 days.
Aims of this study:
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 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
- 否
入选标准
- •Bone resection and endoprosthetic reconstruction for metastatic tumors of the proximal femur or acetabulum
- •Imminent, or de-facto pathologic fractures of proximal femur and/or acetabulum, requiring endoprosthetic reconstruction (with or without bone resection) involving the hip joint
排除标准
- •Pregnant and breast-feeding women
- •Skin defects and wound conditions not amenable to primary wound closure and other DERMABONDTM PRINEOTM contraindications (see 5.1.3.)
- •Underlying infection
- •Total femur replacements
- •Implant revision procedures
研究组 & 干预措施
Prineo
Skin closure with Dermabond Prineo occlusive wound closure system
干预措施: occlusive wound closure (Device)
Staples
Skin closure with staples
干预措施: conventional wound closure (Device)
结局指标
主要结局
Wound status
时间窗: Up to hospital discharge (approximately 1-2 weeks) measured in number of days from intervention
time to dry wound status
次要结局
- Antibiotic Use(Up to hospital discharge (approximately 1-2 weeks) measured in number of days from intervention)
研究者
Werner Hettwer
Consultant Orthopaedic Oncology Surgeon
Rigshospitalet, Denmark
