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临床试验/NCT06735027
NCT06735027招募中不适用

A Randomized Comparative Cohort Study of the Use of Intra-articular Corticosteroid Injection Compared to Suprascapular Nerve Block for Treatment of Shoulder Pain

University of Minnesota1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年1月2日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
change in visual analog scale (VAS) for pain

研究概览

简要总结

The purpose of this study is to evaluate conservative pain relief measures for patients suffering from glenohumeral arthritis or rotator cuff arthropathy. Conservative management of osteoarthritis is often first line treatment, and while a corticosteroid injection is frequently used, suprascapular nerve blocks have not often been described as an analgesic option in this population.

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
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • diagnosis of glenohumeral osteoarthritis, rheumatoid arthritis, or rotator cuff arthropathy who are being offered injection

排除标准

  • uncontrolled diabetes (patients will be excluded if no HbA1c within a year or if it is 8 or greater"
  • known allergy to steroid or anesthetic
  • pregnant women
  • prisoners
  • patients with diminished capacity to consent to participation
  • children under 18 years of age
  • non-English speakers

结局指标

主要结局

change in visual analog scale (VAS) for pain

时间窗: preintervention, 24 hours, 3 days, 1 month, and 3 months postintervention

a validated continuous scale assessment for pain

single assessment numerical evaluation (SANE) of the shoulder

时间窗: preintervention, 24 hours, 3 days, 1 month, and 3 months postintervention

a validated tool providing a numerical score from 0-100 that assess shoulder function as subjectively reported by the subject. A higher score indicates superior shoulder function.

Oxford shoulder score (OSS)

时间窗: preintervention, 24 hours, 3 days, 1 month, and 3 months postintervention

a validated patient-reported outcome measure used to assess shoulder pain and functional disability. Possible scores range from 0-48 with higher scores indicating superior better shoulder function.

American shoulder and elbow surgeons (ASES) score

时间窗: preintervention, 24 hours, 3 days, 1 month, and 3 months postintervention

a validated survey with possible scores from 0-100 that assesses shoulder function as reported by the subject. A higher score indicates superior shoulder function.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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