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临床试验/NCT04607044
NCT04607044终止不适用

Lower Extremity Fixation In Neuropathic Patients Study

Stryker Trauma and Extremities3 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2021年2月3日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
45
试验地点
3
主要终点
Survival Analysis of Implants at 1 Year

研究概览

简要总结

Prospective, multi-site, multi-year post-market clinical follow-up study on neuropathic patients treated/implanted with SALVATION™ External Fixation, SALVATION™ Fusion Bolts and Beams, SALVATION™ Midfoot Nail, The SALVATION™ 3Di Plating System, VALOR™ NAIL, HOFFMANN® LRF SYSTEM and/or T2® ICF SYSTEM of 200 patients with up to 10 sites

详细描述

The selected design is a US, multi-center, multi-year, non-randomized, prospective observational study. The study subjects included are neuropathic patients treated/implanted with SALVATION™ External Fixation, SALVATION™ Fusion Bolts and Beams, SALVATION™ Midfoot Nail, The SALVATION™ 3Di Plating System, VALOR™ NAIL, HOFFMANN® LRF SYSTEM and/or T2® ICF SYSTEM of 200 patients with up to 10 sites.

研究设计

研究类型
Observational
观察模型
Other
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
否

入选标准

  • •Subject is a male or non-pregnant female age 18 years or older at the time of surgery;
  • •Subject is willing and able to give written informed consent and comply with the requirements of this Clinical Investigation Plan (CIP); and
  • •Subject has neuropathy and is intended to be treated for deformity with the one or a combination of the below Systems in accordance with the legally cleared/ approved IFU and Surgical Technique Manual.
  • •HOFFMANN® LRF SYSTEM
  • •SALVATION™ EXTERNAL FIXATION SYSTEM
  • •SALVATION™ FUSION BOLTS AND BEAMS
  • •SALVATION™ 2 MIDFOOT NAIL
  • •SALVATION™ 3DI PLATING SYSTEM
  • •T2® ICF SYSTEM
  • •VALOR™ ANKLE FUSIO NAIL SYSTEM

排除标准

  • •Subjects determined, by the investigator, to be an inappropriate candidate for the procedure indicated;
  • •Unable to consent to participate (written, informed consent);
  • •Unable to attend/complete the requested follow-up visits

结局指标

主要结局

Survival Analysis of Implants at 1 Year

时间窗: 1 years

Compare the pooled cumulative 3-year amputation (above or below the knee) rate of neuropathic patients implanted with SALVATION™ External Fixation, SALVATION™ Fusion Bolts and Beams, SALVATION™ Midfoot Nail, The SALVATION™ 3Di Plating System, VALOR™ NAIL, HOFFMANN® LRF SYSTEM and/or T2® ICF SYSTEM derived from a Kaplan-Meier survival analysis to a performance goal.

次要结局

  • EQ-5D-5L- Index(1 year)
  • FAAM-ADL(1 years)
  • Survival Analysis of Implants at 5 Years(5 years)
  • Radiographic Assessment(5 years)
  • EQ-5D-5L-VAS(1 Year)

研究者

发起方
Stryker Trauma and Extremities
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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