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临床试验/NCT04325789
NCT04325789已完成不适用

A Prospective Randomized Multicenter Evaluation of Rotator Cuff Healing Using a Nanofiber Scaffold in Patients Greater Than 55 Years

Atreon Orthopedics8 个研究点 分布在 1 个国家目标入组 91 人开始时间: 2020年6月29日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
91
试验地点
8
主要终点
Failure of the repair

研究概览

简要总结

Randomized controlled trial of patients over the age of 55 treated with and without a nanofiber scaffold during rotator cuff repair.

详细描述

  1. INTRODUCTION

This document is a protocol for a human research study. This study is to be conducted according to United States standards of Good Clinical Practice in accordance with applicable Federal regulations and institutional research policies and procedures.

Despite numerous advancements in surgical techniques and over 250,000 procedures currently performed annually in the United States, failure of tendon healing following rotator cuff surgery occurs frequently with reports as high as 94%. Nonhealing can lead to persistent pain, poor outcomes, and a significant economic burden to society when revision surgery is required. Several factors have been associated with poor tendon healing with age greater than 60 years shown to be a significant risk factor due to diminishing vascularity at the bone tendon interface where the tear typically originates. While numerous techniques have been devised to improve fixation over the past several decades, very few have been developed to address or enhance the biology at the repair site. Rotium nanofiber is a recent FDA approved scaffold (FDA 510(K) #K183236) that has been shown to improve tendon healing to bone in animal studies. It works to mimic the extracellular matrix and helps concentrates and bind cells at the repair site providing a better organizational structure of the healing tissue. The purpose of the current study is to assess if use of the scaffold significantly improves rotator cuff healing and enhances strength in patients at higher risk of perioperative failure of the repair. 2. BACKGROUND INFORMATION AND SCIENTIFIC RATIONALE

Rotator cuff tears are a frequent cause of shoulder pain and disability in the elderly population. Typically, when conservative measures fail, surgery is often advised. A successful clinical outcome is felt to be heavily predicated on healing of the tendon to the bone. Despite numerous surgical and technical advancements over the past two decades not all repairs heal, with re-tear, or failure-to-heal, remaining the number one complication associated with rotator cuff surgery. This in turn creates a hefty economic burden on society whereupon surgeries are being performed with poor eventual outcomes and ultimately wasted resources.

While reasons for failure are multifactorial, a strong correlation has been associated with advancing age. In an observational study on the natural history of rotator cuff disease, patients younger than 50 years old rarely had rotator cuff tears whereas those greater than 60 had a statistically significant greater incidence of unilateral and bilateral tears. Advancing age is believed to alter and change the intrinsic properties of the tendon leading to stiffness, hypovascularity and overall impairment of the biology of tendon healing. Furthermore, when repairs fail, they typically do so within the first four months of surgery. Means, therefore, to enhance the zone of the repair by increasing the cellularity immediately following surgery may improve the overall healing and lessen failures.

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
Single (Participant)

盲法说明

This is a single blinded study. The patient will be blinded to the treatment group.

入排标准

年龄范围
55 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 55 and older
  • Able to provide informed consent
  • Primary diagnosis of rotator cuff tear

排除标准

  • Revision rotator cuff surgery
  • Partial thickness rotator cuff tears
  • Massive (greater than 5cm) rotator cuff tears
  • Patients with current tobacco history

研究组 & 干预措施

Group 1 Control

No Intervention

Group 1 will serve as the control and undergo routine rotator cuff repair with suture anchors without the nanofiber scaffold.

Group 2 Scaffold

Active Comparator

Group 2 will undergo rotator cuff repair with suture anchors and incorporation of the nanofiber scaffold.

结局指标

主要结局

Failure of the repair

时间窗: 24 months

To determine if the use of the nanofiber scaffold changes the occurrence of postoperative rotator cuff repair (RCR) failure in patients older than 55 years

次要结局

  • Change in shoulder range of motion(Preoperative, 6 weeks, 3 months, 6 months, 12 months, 24 months postoperative)
  • Change in patient-reported Single Assessment Numeric Evaluation (SANE) score(Preoperative, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months postoperative)
  • Change in patient-reported American Shoulder and Elbow Scores(Preoperative, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months postoperative)
  • Change in patient-reported Veteran Rand 12 (VR-12) score(Preoperative, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months postoperative)
  • Change in isometric rotator cuff muscle strength peak force(Preoperative, 3 months, 6 months, 12 months, 24 months postoperative)
  • Change in patient-reported postoperative pain (Visual Analogue Scale - Pain)(Preoperative, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months postoperative)

研究者

发起方
Atreon Orthopedics
申办方类型
Industry
责任方
Sponsor

研究点 (8)

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