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临床试验/NCT04084262
NCT04084262已完成不适用

Correction of Multi-Plane Hallux Valgus Deformity Using the Phantom® Intramedullary Nail

Paragon 281 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2019年11月7日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Paragon 28
入组人数
12
试验地点
1
主要终点
Change in Frontal Plane Rotation

研究概览

简要总结

The goal of this research study is to determine the change in frontal plane rotation of the 1st metatarsal from pre to post arthrodesis of the 1st TMT joint with the Phantom® Intramedullary Nail combined with a supinating reduction technique.

The study hypothesis is that multi-planar correction can be achieved with the Phantom® Intramedullary Nail.

详细描述

Each subject will undergo a Lapidus Arthrodesis combined with a supinating reduction technique.

The subjects will undergo 3 weight-bearing CBCT scans of their foot and ankle, one pre-arthrodesis, one two weeks post-arthrodesis, and one 12 weeks post-arthrodesis. These scans will be used to determine change in frontal plane rotation of the 1st metatarsal from pre to post arthrodesis of the 1st TMT joint, change in angular/positional alignment of the 1st TMT joint using various measurements (1-2 IMA, Meary's Angle, HVA, MAA, Sesamoid Position, and Sesamoid Frontal Plane Rotation), maintenance of correction of the 1st TMT joint, and union status.

The subjects will also complete three surveys, the Pain and Satisfaction Survey, the AOFAS Hallux MTP-IP Scale, and the FAOS Foot and Ankle Survey, at the Pre-Operative Visit, 2 Week Visit (post-op), 6 Week Visit (post-op), and 12 Week Visit (post-op). Furthermore, the subjects will be asked about their willingness to undergo the procedure again at the 12 Week Visit (post-op). All of these scores will be considered in the secondary objectives.

Aside from the study activities listed above, all procedures, visits, and instructions for the subject are to follow the standard of care.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

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 subject is at least 18 years of age at the time of screening.
  • The subject has been diagnosed with hallux valgus.
  • The subject has pain associated with hallux valgus.
  • The subject agrees to comply with the requirements of the study and complete the study measures.
  • The subject is willing and able to provide written informed consent.
  • The subject plans to undergo a Lapidus Arthrodesis procedure with a 3-Hole Phantom® Intramedullary Nail.

排除标准

  • The subject is pregnant.
  • The subject has had previous surgery for hallux valgus on operative side.
  • The subject will require a structural graft in the 1st TMT joint.
  • The unshod foot in question is greater than 28 cm in length.
  • The subject is not expected to complete the study according to the investigation plan.
  • The subject has been deemed physiologically or psychologically inadequate by the enrolling physician.
  • The subject is a prisoner, unable to understand what participation in the study entails, mentally incompetent, a known abuser of alcohol and/or drugs, or anticipated to be non-compliant.

结局指标

主要结局

Change in Frontal Plane Rotation

时间窗: 12 weeks

Determine the change in frontal plane rotation of the 1st metatarsal from pre to post arthrodesis of the 1st tarsometatarsal joint with the Phantom® Intramedullary Nail combined with a supinating reduction technique.

次要结局

  • Clinical Complications(Pre-Op, 2 weeks, 6 weeks,12 weeks)
  • Patient Current Level of Pain at Surgical Site(Pre-Op, 2 weeks, 6 weeks, 12 weeks)
  • Meary's Angle(Pre-op, 2 weeks, 12 weeks)
  • Sesamoid Frontal Plane Rotation(Pre-op, 2 weeks, 12 weeks)
  • FAOS(Pre-Op, 2 weeks, 6 weeks, 12 weeks)
  • Union Status(12 weeks)
  • Metatarsus Adductus Angle(Pre-op, 2 weeks, 12 weeks)
  • Sesamoid Position(Pre-op, 2 weeks, 12 weeks)
  • Maintenance of Correction(Pre-op, 2 weeks, 12 weeks)
  • AOFAS(Pre-Op, 2 weeks, 6 weeks, 12 weeks)
  • Patient Satisfaction with Procedure(Pre-Op, 2 weeks, 6 weeks, 12 weeks)
  • Willingness to Undergo Procedure Again(12 weeks)
  • 1-2 Inter Metatarsal Angle(Pre-op, 2 weeks, 12 weeks)
  • Hallux Valgus Angle(Pre-op, 2 weeks, 12 weeks)

研究者

发起方
Paragon 28
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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