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临床试验/NCT03883737
NCT03883737已完成不适用

Effect of the Ultrasound-guided Percutaneous Neuromodulation on the Anterior Pain Knee: a Pilot Study

University of Seville1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2019年4月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
1
主要终点
range joint

研究概览

简要总结

Anterior knee pain (AKP) is one of the most frequent pathologies of the lower limb, in young and adult subjects. In the field of Physiotherapy, ultrasound-guided Percutaneous Neuromodulation (PNM) is defined as the application through a needle with ultrasound guidance of an electrical current at low or medium frequency, seeking a sensitive and / or motor response of a peripheral nerve in some point of its trajectory, or of a muscle in a motor point, with a therapeutic objective. The objective of this study is to analyze that the effect of PNM on the femoral nerve produces statistically significant changes in pain, joint range and knee functionality in patients with chronic AKP. Thirty subjects will be recruited, which will be divided into 2 groups: group 1 to which PNM will be applied to the femoral nerve of the pain knee; and group 2 to which PNM will be applied to the femoral nerve of the non-pain knee. The PNM intervention with NMP will consist in the single application of an asymmetric rectangular biphasic current (250 microseconds, 10 Hz)

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •chronic anterior knee pain >3 months
  • •older than 18 years-old

排除标准

  • •Surgical intervention in the intervention area
  • •Prosthesis or osteosynthesis in the intervention area
  • •Cardiac or tumoral diseases
  • •Coagulopathies
  • •Be under the effects of certain medications
  • •contraindication characteristic of the puncture

研究组 & 干预措施

Group 1: PNM in pain knee

Experimental

participants in whom PNM will be applied to the femoral nerve of the pain knee

干预措施: PNM (Other)

Group 2: PNM in non-pain knee

Experimental

participants in whom PNM will be applied to the femoral nerve of the non-pain knee

干预措施: PNM (Other)

结局指标

主要结局

range joint

时间窗: up to 1 week

goniometer

visual analog scale (VAS) (0, no pain; 100, maximum pain).

时间窗: up to 1 week

pain

Kujala questionnaire (0, maximum pain; 100, no pain).

时间窗: up to 1 week

Functional pain

VISA-p questionnaire (0, maximum pain; 100, no pain).

时间窗: up to 1 week

Functional pain

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Blanca de la Cruz Torres

Director

University of Seville

研究点 (1)

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