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临床试验/NCT06386926
NCT06386926尚未招募不适用

Radial Shockwave Versus Ultrasound Phonophoresis in Management of Chronic Supraspinatus Tendinitis

Cairo University1 个研究点 分布在 1 个国家目标入组 69 人开始时间: 2024年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
69
试验地点
1
主要终点
Change in shoulder range of motion

研究概览

简要总结

Comparative study to compare the effect of radial shockwave versus ultrasound phonophoresis in management of chronic supraspinatus tendinitis consists of 3 groups exp1(shockwave treatment + conventional physical therapy) , exp2( ultrasound phonophoresis+ conventional physical therapy) and control group ( conventional physical therapy)

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • BMI 18.5-24.9
  • 18 years to 60
  • with Unilateral Chronic Supraspinatus Tendinitis.
  • Tenderness is found over the supraspinatus as it passes sub-acrominal and anterolateral.
  • The patient reported with positive Jobe's test (empty can test)
  • The patient reported pain with active shoulder elevation in the scapular plane (eg: welders, plate workers, slaughterhouse workers and overhead playing athletes).
  • The patient reported pain with resisted isometric abduction

排除标准

  • Case reports, treatments after surgery, did not meet our specified outcome parameters, traumatic incidents,
  • Partial tears at surgery
  • Massive retracted tears at surgery
  • Frozen shoulder.
  • Rotator cuff tear.
  • Glenohumeral or acromioclavicular arthritis

结局指标

主要结局

Change in shoulder range of motion

时间窗: before start of treatment and 4 weeks following end of treatment

electro goniometer

change in pain intesity

时间窗: before start of treatment and 4 weeks following end of treatment , score from 0-10 ,0=no pain , 10= unbearable pain

VAS ( visual analog scale score)

change in the thickness of supraspinatus tendon

时间窗: before start of treatment and 4 weeks following end of treatment

Ultrasonography

次要结局

  • measure weight in kg and height in cm(before starting the assessment)
  • Function of the Upper Limb(before start of treatment and 4 weeks following end of treatment, it measure the disability/symptom section (11 items, scored 1-5))

研究者

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

Shady Bahaaldin Alkadry

Physical therapist

Cairo University

研究点 (1)

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