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临床试验/NCT06029413
NCT06029413已完成不适用

Myo Vs. Myofascial Injection for Myofascial Trigger Points. Is There Really a Difference? A Randomized Controlled Trial

Bozyaka Training and Research Hospital2 个研究点 分布在 2 个国家目标入组 76 人开始时间: 2023年9月26日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
76
试验地点
2
主要终点
VAS(Visual Analog Scale)

研究概览

简要总结

In this study, the effectiveness of two different application methods that can be used in myofascial trigger point injection treatment will be compared.

详细描述

This study aims to compare the intramuscular trigger point injection, which is traditionally used in the treatment of myofascial trigger points with the method in which facial layers are also included in the application.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Pain in the upper back area
  • Detection of active trigger point in upper back muscles (trapezius, levator scapula, rhomboids, supraspinatus and infraspinatus)
  • Presence of at least two of the three criteria recommended for the diagnosis of trigger point:
  • Hypersensitive point
  • Referred pain
  • Pain VAS score ≥ 4
  • Between the ages of 18-65 -

排除标准

  • Using analgesics or anti-inflammatory medicines.
  • Having received physical therapy for the same symptoms in the past 3 months
  • Serious psychiatric illness
  • Presence of malignancy or infection
  • Coagulation disorder
  • History of operation in the relevant region
  • Presence of fibromyalgia syndrome
  • History of allergy to local anesthetics

结局指标

主要结局

VAS(Visual Analog Scale)

时间窗: 1 week after intervention

Pain intensity will be evaluated with the visual analog scale (VAS). VAS is a scale used to digitize subjective values such as behavior or characteristics that cannot be measured directly. Two end definitions of the parameter to be evaluated are written on both ends of a 10 cm line and the patient is asked to indicate where his/her condition is appropriate on this line by drawing a line (0. : no pain, 10: very severe pain)

次要结局

  • Functional Status(1 week after intervention)
  • Pressure Pain Threshold(1 week after intervention)

研究者

发起方
Bozyaka Training and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Buğra İnce

Assoc. Professor, MD

Bozyaka Training and Research Hospital

研究点 (2)

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