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临床试验/NCT05427916
NCT05427916终止不适用

Prospective Randomized Evaluation of the Effect of Avance® Solo Negative Pressure Wound Therapy System or Optifoam® Gentle Post-Op Dressing on "High Risk" Closed Surgical Incisions; Freedom From Wound Complication Study

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2022年7月12日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
20
试验地点
1
主要终点
Number of Participants With Healing Complication

研究概览

简要总结

The primary objective is to assess the frequency of a wound healing complication, in a closed incisional wound in a "high risk" surgical incision when treated with Negative Pressure Wound Therapy versus a highly absorbent antimicrobial post - operative absorbent dressing.

详细描述

A healing complication is defined as presence of at least one of the following conditions: infection (superficial or deep), dehiscence (partial, superficial, or deep), or delayed healing (incision not 100% closed within 7 days of the first surgical procedure), drainage form the wound after 96 hours post operatively.

The secondary objectives are to assess any changes in the following assessments of the surgical incision weekly over the treatment period:

  • Surrounding skin condition
  • Incision complications, infection or clinical signs of infection
  • to assess the number and type of these complications individually including other postsurgical complications: skin necrosis, cellulitis, abscess, suture abscess, seroma, periwound edema or hematoma occurring within 21, 42, and 90 days postoperatively
  • Pain during dressing changes

Assessment of the following at dressing changes:

  • Duration/wear time
  • Ease of use; difficulty with sleep
  • Damage to surrounding skin on removal
  • Assessment of re-epithelialization/closure
  • Patient comfort during wear; ease of ambulation
  • Conformability of dressing
  • Exudate management
  • Reasons for removal

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

入选标准

  • The patient must be at least 18 years of age.
  • Males and females - provided they are not pregnant and if of reproductive age are using contraception.
  • Have a closed surgical incision post-surgery/closure (<24 hours after).
  • The patient is able to understand the evaluation and is willing to consent to the evaluation.
  • Undergoing appropriate: wound "high risk" surgery.
  • Foot and ankle surgery.
  • Vascular groin incision.
  • Long leg vein harvest incision.
  • Closed forefoot and major amputation surgery.
  • Possibly: breast augmentation and reduction surgery.
  • HIV and hepatitis positive patients will not be excluded from this study.
  • Renal failure patients will not be excluded.
  • Patient on metabolic agent, immunosuppressants, or steroid therapy will not be excluded from this study.

排除标准

  • Incisions in excess of effective dressing pad size provided.
  • Patients with a known history of poor compliance with medical treatment.
  • Patients who have participated in this trial previously and who were withdrawn.
  • Patients with known allergies to product components (silicone adhesives and polyurethane films (direct contact with incision), acrylic adhesives (direct contact with skin), polyethylene fabrics and super-absorbent powders (polyacrylates) (within the dressing).
  • Incisions where daily inspection is required underneath the dressing.
  • Incisions which have an infection which is not being treated with systemic antibiotics.
  • Incisions which are actively bleeding.
  • Exposure of blood vessels, organs, bone or tendon at the base of the reference incision.

结局指标

主要结局

Number of Participants With Healing Complication

时间窗: 21 days

Healing complications are defined as the presence of at least one of the following conditions: infection (superficial or deep), dehiscence (partial, superficial, or deep), or delayed healing (incision not 100% closed within 7 days of the first surgical procedure)

次要结局

  • Number of Skin Necrosis Complications(90 days)
  • Number of Seroma Complications(90 days)
  • Pain During Dressing Changes(90 days)
  • Number of Cellulitis Complications(90 days)
  • Number of Abscess Complications(90 days)
  • Number of Hematoma Complications(90 days)
  • Number of Suture Abscess Complications(90 days)
  • Number of Periwound Edema Complications(90 days)
  • Patient Satisfaction(90 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

John Lantis

Professor

Icahn School of Medicine at Mount Sinai

研究点 (1)

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