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临床试验/NCT00971451
NCT00971451Unknown不适用

Quadriceps Function Prior to Anterior Cruciate Ligament Reconstruction

University of Virginia2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2007年11月最近更新:
适应症

试验速览

阶段
不适用
入组人数
50
试验地点
2
主要终点
Quadriceps muscle strength and inhibition using the quadriceps central activation ratio

研究概览

简要总结

Patients who are diagnosed with an isolated tear of the anterior cruciate ligament and scheduled for arthroscopic reconstruction using bone-patellar tendon-bone autograft will be recruited to participate.

All subjects will be invited to participate in 2 weeks (2 supervised sessions per week) prior to their surgery. Each session will include supervised therapeutic exercises. Subjects will be randomly assigned to receive continuous transcutaneous electrical nerve stimulation (TENS) during each session or knee joint cryotherapy prior to each exercise session. The investigators will measure quadriceps function before and after this 2-week intervention (both sessions occur prior to reconstruction surgery). This study will also have a true control group that will not receive either exercise of modality intervention. The investigators will collect subjective and objective outcomes data at regularly scheduled post-operative visits.

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 (Outcomes Assessor)

入排标准

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

入选标准

  • Complete ACL rupture

排除标准

  • Persons who cannot tolerate knee joint TENS.
  • Persons who have a known allergy to cryotherapy
  • Patients who are pregnant or who plan on getting pregnant during the 12-month follow-up period.

结局指标

主要结局

Quadriceps muscle strength and inhibition using the quadriceps central activation ratio

时间窗: Day 15

次要结局

  • Quadriceps H-reflex testing(Day 15)
  • International Knee Documentation Committee Subjective Knee Joint Evaluation(Day 15)
  • Visual Analog Scale(Day 15)
  • Tegner Activity Rating(Day 15)

研究者

申办方类型
Other

研究点 (2)

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