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临床试验/NCT06080334
NCT06080334已完成不适用

Effectiveness of Dry Needling of the Gastrocnemius Muscle vs. Electrolysis in Subjects With Achilles Tendinopathy: a Randomised Single-blind Clinical Trial

Universidad Católica de Ávila2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2023年12月1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
入组人数
80
试验地点
2
主要终点
Pain intensity.

研究概览

简要总结

Achilles tendinopathy is the injury that primarily occurs in athletes and people who engage in repetitive activities that involve the calf muscles, such as running, jumping, and sudden acceleration and deceleration movements. To observe the effectiveness of dry needling in the PGM of the gastrocnemius muscle, in the short and medium term, on the intensity of pain in gastrocnemius muscle, in the short and medium term, on pain intensity in patients with patients with Achilles tendinopathy, compared to the application of ultrasound-guided percutaneous electrolysis on the tendon.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Signing of informed consent both to participate in the study and to undergo invasive in the study, as well as to undergo invasive physiotherapy techniques. physiotherapy techniques.
  • Presence of symptoms (swelling or pain) for at least 3 months.
  • Positive Achilles tendon palpation test.
  • Males and females over 18 years of age.
  • Presence of MMP in the gastrocnemius muscle, meeting at least three of the following criteria diagnostic criteria described by Travell and Simons:
  • Presence of palpable tight band.
  • Local pain on pressure at the nodule of the tense band.
  • Recognition by the patient as his usual pain after mechanical after mechanical stimulation of the sensitive nodule.
  • Limitation of range of motion.

排除标准

  • Any related acute or chronic musculoskeletal disease that may related chronic musculoskeletal disease, which may affect the results of the study

结局指标

主要结局

Pain intensity.

时间窗: 5 weeks

Measurement of pain intensity using the VAS scale (0 minimum pain, 10 maximum bearable pain).

次要结局

  • Pressure pain threshold(5 weeks)
  • Range of movement(5 weeks)

研究者

发起方
Universidad Católica de Ávila
申办方类型
Other
责任方
Principal Investigator
主要研究者

JORGE VELAZQUEZ SAORNIL

Principal investigator

Universidad Católica de Ávila

研究点 (2)

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