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临床试验/NCT04897308
NCT04897308已完成不适用

Shoulder Adhesive Capsulitis ; Comparison Between Three Theraputic Approaches

Sohag University1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2021年5月1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
54
试验地点
1
主要终点
Improvement in range of motion of shoulder joint

研究概览

简要总结

This study will compare between the effect of three treatment modalities of shoulder adhesive capsulitis to hilight the best technique to improve pain and range of motion outcome measures .

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
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •gross limitation of passive shoulder movement
  • •pain interfering with daily activities
  • •painful restiction of active and passive movement of shoulder

排除标准

  • •presence of degenerative pathology
  • •contraindication to steroid injection
  • •deformity affecting upper limb
  • •history of previous shoulder injection in the past 4 weeks

研究组 & 干预措施

Suprascapular nerve block

Active Comparator

This group will include will under go suprascapularnerve block as following :10 ml of .5% bupivacaine and 2 ml of methylpradnisolon 40mg/ml

干预措施: Local injection of shoulder joint (Procedure)

Hydrodilatation of shoulder capsule

Active Comparator

This group will undergo intraarticular hydrodilatation by injection of :first lidocaine10ml%followed by 1ml of methylprednisolon 40mg/ml and finally 20ml of .9 % sodium chloride slowly in the gleno humeral joint

干预措施: Local injection of shoulder joint (Procedure)

Hydrodilatation of shoulder interval

Active Comparator

This group will undergo interval hydrodilatation by injection of :first mepivacaine 10ml folowed by 20ml of sterile water slowly in the shoulder interval

干预措施: Local injection of shoulder joint (Procedure)

结局指标

主要结局

Improvement in range of motion of shoulder joint

时间窗: 12 weeks efter intervention

Improvement will be measured by measuring active and passive range of motion

Improvement in pain

时间窗: 12 weeks after intervention

Improvement will be measured by VAS ( visual auditory assessment )

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

Shorouk Ayman Mohamed

Resident doctor

Sohag University

研究点 (1)

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