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临床试验/PACTR201602001462295
PACTR201602001462295招募中未知

DRY NEEDLING VERSUS ISCHEMIC COMPRESSION IN TREATMENT OF LOWER BACK MYOFASCIAL PAIN SYNDROME

amr moustafa yehia0 个研究点目标入组 60 人开始时间: 2016年2月7日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Year(s) 至 45 Year(s)(—)
性别
All

入选标准

  • ¿Age ranges from 18 to 45 years old
  • ¿Patients with lower back myofascial pain syndrome that has been diagnosed by orthopedist.
  • ¿Pain of at least 30 mm to 70 mm on a visual analogue scale (VAS) from 0 mm (no pain) to 100 mm (worst imaginable pain)
  • ¿Patients able to perform (ROM) test of Lumbar Spine (flexion, extension and side binding) but limited before treatment.
  • ¿Presence of active or latent MTrPs at least 4 trigger points.
  • ¿Patients had lower back myofascial pain syndrome for at least 3 months ago.

排除标准

  • ¿History of previous back surgery.
  • ¿Neurologic deficit.
  • ¿Current lower extremity symptoms.
  • ¿Cardiopulmonary disease with decreased activity tolerance.
  • ¿Rheumatologic conditions such as mild systemic lupus erythematosus, polyarticular osteoarthritis, rheumatoid arthritis and advanced lumbar degenerative disease.
  • ¿Participants receiving other treatment, in the form of physical therapy or medication, for the duration of the study that may interfere with the results of this study.
  • ¿Bleeding disorders.
  • ¿Renal disorders.
  • ¿Disc lesion.

研究者

发起方
amr moustafa yehia

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