跳至主要内容
临床试验/NCT05474898
NCT05474898Unknown不适用

Magnesium Sulphate Iontophoresis Versus High- Power Pain Threshold Ultrasound in Mechanical Neck Pain

Cairo University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2022年8月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
90
试验地点
1
主要终点
pain intensity

研究概览

简要总结

to investigate the effects of Magnesium Sulphate Iontophoresis versus High Power Pain Threshold Ultrasound on pain, function and range of motion on active MTrPs found in the upper trapezius.

详细描述

Myofascial pain syndrome (MPS) is a musculoskeletal chronic pain disorder that affects the majority of pain population and characterized by the presence of trigger points. MPS is usually associated with tenderness, spasm, movement limitation and referred pain .

Myofascial trigger points (MTrPs) are hyperirritable taut fibers of skeletal muscle. The taut fibers within the muscle create palpable nodules that may cause local pain, and refer pain elsewhere with soft tissue examination .

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 (Participant)

入排标准

年龄范围
19 Years 至 23 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Subjects, with age ranged from 19-23 years (Forman et al, 2014) from both genders. The subjects had active MTrPs in the upper fibers of trapezius muscle.

排除标准

  • •• History of whiplash injury.
  • •History of cervical spine surgery.
  • •Cervical radiculopathy or myelopathy.
  • •Having undergone physical therapy within the past three months before the study.
  • •Non- rheumatologic diseases as multiple sclerosis, thyroid dysfunction and chronic infection.
  • •Rheumatologic condition as poly-articular osteoarthritis, rheumatoid arthritis and advanced cervical spine degenerative diseases.

研究组 & 干预措施

Group (A)

Experimental

干预措施: Magnesium Sulphate Iontophoresis +conventional therapy (Other)

Group (A)

Experimental

干预措施: conventional theapy (Other)

Group (B)

Experimental

干预措施: High- Power Pain Threshold Ultrasound +conventional therapy (Other)

Group (B)

Experimental

干预措施: conventional theapy (Other)

Group (c)

Other

干预措施: conventional theapy (Other)

结局指标

主要结局

pain intensity

时间窗: up to four weeks

The scale that will be used the VAS ;each subject will instructed to put point on line from no pain to tolerable pain

次要结局

  • neck disability(up to four weeks)
  • range of motion(up to four weeks)
  • Pain pressure threshold (PPT)(up to four weeks)

研究者

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

Hend Hamdy

lecturer of pt for basic science department

Cairo University

研究点 (1)

Loading locations...

相似试验