跳至主要内容
临床试验/ISRCTN11696305
ISRCTN11696305已完成不适用

Study to compare the effects of steroid injection vs steroid injection and hydrodilatation in the treatment of adhesive capsulitis: a randomised control trial

Joint Research Office (part of the Research Support Centre) UC0 个研究点目标入组 170 人开始时间: 2015年5月2日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
170

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

性别
All

入选标准

  • 1. Clinical diagnosis of adhesive capsulitis
  • 2. Normal radiograph of the shoulder
  • 3. Restriction of range of motion compared to unaffected shoulder of at least 30 degrees in 2 of three movements; forward flexion, abduction, and external rotation in neutral measured with a goniometer.
  • 4. Able to give informed consent
  • 5. Diabetic, thyroid or post traumatic (e.g. post dislocation) causes may be included (otherwise slower to recruit numbers).
  • 6. Symptoms for any period of time as long as it can be recorded
  • 7. All patients presenting with adhesive capsulitis should be considered for the trial, but it’s the clinician’s choice if they wish to offer other treatments.

排除标准

  • 1. Patients unable to complete questionnaires
  • 2. Patients under 18 or over 85
  • 3. Any surgical intervention for adhesive capsulitis already performed
  • 4. Pre-existing major trauma or surgery to the shoulder
  • 5. Patients with known or suspected musculoskeletal infection in affected shoulder
  • 6. Patients with known or suspected malignancy
  • 7. Steroid injection to affected shoulder less than six weeks at time of proposed intervention
  • 8. Patient on oral steroids
  • 9. Azathioprin, other DMD disease modifying drugs and medication taken after the intervention, in the periods of 6 weeks and 3 months.

研究者

发起方
Joint Research Office (part of the Research Support Centre) UC

相似试验