跳至主要内容
临床试验/NCT04827303
NCT04827303已完成不适用

Effectiveness of 3 Different Methods in Acute Myofascial Pain Syndrome: A Randomized Controlled Study

Ufuk University1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2017年4月1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
75
试验地点
1
主要终点
Visual analog scale

研究概览

简要总结

This study is a randomized controlled study. A total of 75 patients between the ages of 20-50 who have a diagnosis of acute myofacial pain syndrome in the trapezius muscle and have pain for a maximum of 5 days were included in the study. Patients were randomly divided into 3 groups. Group 1 patients received kinesio tape method (25 patients), group 2 patients received trigger point injection method (25 patients), and group 3 patients received neural therapy injection method (25 patients). A 10-15 cm sized I band was applied to the trapezius muscles of the first group patients with the patient's neck in lateral flexion. Then, while the patient's neck is flexed, a Y-shaped 15-20 cm tape will be affixed between C1-7 with the arms of the Y up, and I tape of 5-10 cm is attached on the arms. In group 2 patients, 1 cc lidocaine diluted with 4 cc saline (SF) was applied to the trigger points palpated manually in the trapezius muscles. After the trigger point was squeezed between the thumb and index finger, a few cc of local anesthetic mixture was applied into the trigger point with the injector and exited. In the 3rd group patients, a few cc local anesthetic mixture will be applied intradermally over the trigger point without entering into the trigger points palpated manually in the trapezius muscles. Patients were checked 72 hours and 1 week after the first applications.

The pain at rest and during movement of the patients in all 3 groups were evaluated with a visual analog scale (VAS 10 cm). The number of trigger points was determined by the physician by hand palpation. Pressure pain threshold was evaluated with the algometer device. Disability assessment of the patients was made using the neck pain disability index. evaluations were made at the beginning of treatment, 72 hours after and 1 week after treatment.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients diagnosed with acute myofascial pain syndrome
  • Patients between the ages of 20-50
  • Patients with pain for up to 5 days

排除标准

  • Patients diagnosed with fibromyalgia
  • Patients with systemic disease
  • Patients with prominent cervical disc herniation
  • Patients with cervical arthrosis
  • Patients with cervical radiculopathy and myelopathy
  • Patients with myofascial trigger point injection in the past 6 months
  • Patients who received physical therapy in the past 6 months
  • Patients undergoing shoulder and neck surgery
  • Patients with drug allergies

结局指标

主要结局

Visual analog scale

时间窗: 1 week

The pain at rest and during movement of the patients in all 3 groups were evaluated with a visual analog scale (VAS 10 cm).

The number of trigger points

时间窗: 1 week

The number of trigger points was determined by the physician by hand palpation.

Neck pain disability index

时间窗: 1 week

Disability assessment of the patients was made using the neck pain disability index.

Pressure pain threshold

时间窗: 1 week

Pressure pain threshold was evaluated with the algometer device.

次要结局

未报告次要终点

研究者

发起方
Ufuk University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Saime Ay

Professor Doctor

Ufuk University

研究点 (1)

Loading locations...

相似试验