跳至主要内容
临床试验/NCT04403919
NCT04403919已完成不适用

Knotless Suture in Revision Total Joint Arthroplasty: A Prospective Randomized Controlled Trial

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2020年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
81
试验地点
1
主要终点
Time of Closure in Minutes

研究概览

简要总结

Barbed suture has been demonstrated to be safe in primary hip and knee surgery and retrospective data suggests barbed suture represents no increased complications in the revision setting. Barbed suture may represent a faster, more effective way to perform revision arthroplasty closures. There are no Level I studies comparing traditional and barbed suture closure. The purpose of this study is to assess the surgical complexities of closures using closure time without sacrificing cosmesis or wound complications between the traditional closure and barbed closure.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
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

  • •Patients ≥ 18 years of age
  • •Surgical candidates undergoing revision total knee or total hip arthroplasty for one of the following indications second stage of two stage reimplantation for infection, mechanical loosening, instability, polyethylene wear, stiffness, or periprosthetic fracture

排除标准

  • •Patient is ≤ 18 years of age
  • •Patient is unable to provide written consent
  • •Patient has active infections in the operative leg/joint
  • •Known Allergy to Suture material
  • •Underlying Dermatological diseases affecting surgical site including dermatitis, eczema, or psoriasis; connective tissue or vascular disorders or diseases that would adversely affect wound healing; metastatic cancer; renal insufficiency (dialysis); steroid dependence; malnourishment; and other disease processes resulting in an immunocompromised state. Diabetes, smoking and obesity will be allowed as they are frequent comorbidities in our revision joint population
  • •Anterior total hip replacement
  • •Stage 1 of two stage revision for infection
  • •Closure performed by plastic surgeon, including flap coverage
  • •Vulnerable populations will not be enrolled in this study.
  • •Withdrawal Criteria
  • •Failure to attend regularly scheduled follow up appointments
  • •Deviation from closure protocol

研究组 & 干预措施

Revision total knee arthroplasty: control

Active Comparator

干预措施: Conventional Closure: Knee (Device)

Revision total knee arthroplasty: active

Experimental

干预措施: Barbed suture closure: Knee (Device)

Revision Total Hip Arthroplasty: control

Active Comparator

干预措施: Conventional Closure: Hip (Device)

Revision Total Hip Arthroplasty: active

Experimental

干预措施: Barbed suture closure: Hip (Device)

结局指标

主要结局

Time of Closure in Minutes

时间窗: Up to a maximum of 66 minutes (perioperative)

Measurement of the time needed to properly close the wound with each technique.

次要结局

  • Mean Length of Incision(30 minutes (perioperative))
  • Mean Number of Sutures Used(45 minutes (perioperative))
  • Incidence of Complications Related to Wound Closure(Day 90)
  • Patient and Observer Scar Assessment Scale (POSAS) Score(Week 6 Post-Surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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