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临床试验/NCT06139276
NCT06139276尚未招募不适用

Outcomes of a Specially Designed Needle (Small Needle-Knife) Treating Frozen Shoulder Based on Analysis of Microcirculation and Pulse Changes

Taipei City Hospital0 个研究点目标入组 120 人开始时间: 2024年1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
120
主要终点
Pain VAS

研究概览

简要总结

The aim is to investigate whether adding small needle-knife therapy to standard Western medicine enhances the treatment of frozen shoulder by evaluating its impact on microcirculation and meridian unblocking.

详细描述

The aim of this research is to investigate whether the combination of small needle-knife therapy with conventional Western medicine treatment can enhance therapeutic effects compared to conventional treatment methods. In addition to clinical measurements of joint mobility and relevant scales, this study integrates instruments such as Laser Doppler Flowmetry (LDF) and pulse diagnosis devices. These non-invasive methods are employed to evaluate the microcirculation performance of patients with frozen shoulder before and after conventional Western medicine treatment or combined treatment with small needle-knife therapy. The objective is to understand the effects of small needle-knife therapy on the microcirculation and meridian unblocking in frozen shoulder patients.

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 (Outcomes Assessor)

入排标准

年龄范围
40 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Limited shoulder joint mobility in various angles (forward flexion, abduction, external rotation, and internal rotation), persisting for over two months.
  • Persistent pain on the affected shoulder even without rest.
  • Willing and consenting to participate in this research.

排除标准

  • Degenerative shoulder joint arthritis (osteoarthritis).
  • Rheumatoid arthritis.
  • Fracture of the humerus, clavicle, scapula, shoulder acromioclavicular dislocation, shoulder dislocation.
  • Cervical radiculopathy.
  • Thoracic outlet syndrome.
  • Restricted shoulder joint mobility due to stroke, spinal cord injury, or other factors.

结局指标

主要结局

Pain VAS

时间窗: 90 days

The intensity of the pain along a continuum from 'no pain' to 'worst pain' imaginable with visual analog scale.

ROM

时间窗: 90 days

Glenohumeral range of motion(ROM) of the affected shoulder.

次要结局

  • BPW(90 days)
  • LDF(90 days)
  • WHOQOL-BREF(90 days)
  • SPADI(90 days)
  • PPG(90 days)

研究者

申办方类型
Other Gov
责任方
Sponsor

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