跳至主要内容
临床试验/NCT03943329
NCT03943329已完成不适用

Trial of a Distal Targeting System for Cephalomedullary Nails as Part of Surgical Repair of Hip and Femoral Shaft Fractures

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年12月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Change in mean intra-operative radiation exposure to patients during their cephalomedullary nailing procedure.

研究概览

简要总结

This study will be a prospective, case - control trial looking at the use of a previously FDA approved device made by Stryker, a distal targeting system that eases the distal targeting of screws in cephalomedullary nails in hip and femoral shaft fractures. Patients who consent to participate in the study will either be in the control or device arm of the study depending on their surgeon.

详细描述

Surgeries conducted by Dr. Konda or Dr. Leucht will be done using the device technique, surgeries completed by Dr. Egol or Dr. Tejwani will be done without the device, "free hand" technique. Each arm of the study will contain 29 patients. Patients who consent to participation will be enrolled in the study and placed in the correct arm based on who their surgeon is. Demographic and injury data will be collected. Intra-operatively, control patients will receive the SOC procedure. Device arm patients will have the distal targeting device used in their procedure, but the implant, will not be different than SOC.

研究设计

研究类型
Interventional
分配方式
Non 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

入选标准

  • The patient must be greater than or equal to 18 years of age.
  • The patient must have sustained a hip or femur fracture that is indicated for cephalomedullary nailing as the primary and definitive treatment measure.
  • The patient must be medically cleared for operative fixation of their fracture.

排除标准

  • The patient does not meet all of the inclusion criteria.

结局指标

主要结局

Change in mean intra-operative radiation exposure to patients during their cephalomedullary nailing procedure.

时间窗: Baseline, 1 Day

次要结局

  • Change in mean length of time to distal screw placement(Baseline, 1 Day)
  • Change in total operative time(Baseline, 1 Day)
  • Change in total operative cost ($)(Baseline, 1 Day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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