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临床试验/NCT03870191
NCT03870191已完成不适用

Comparison of Therapeutic Effects of Trigger Point Injection and Twin Nerve Block in Chronic Myofascial Pain Patients

Rutgers University0 个研究点目标入组 48 人开始时间: 2016年6月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
48
主要终点
Pain relief: numerical pain scale

研究概览

简要总结

To see if there is there any difference in the treatment outcomes/results such as changes in pain intensity in patients with myofascial pain who have been treated with trigger point injections or twin block?

详细描述

Most treatment approaches for chronic myofascial pain are not evidence-based. Studies are usually controversial. Most are short-term, non-randomized. An essential limitation has been the lack of standardization of diagnosis. Some studies do not differentiate between joint pain and muscle pain, which can significantly affect the outcome of the treatment provided.

Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) was recently published and validated. Their protocol allows standardization of the assessment and diagnosis of patients with temporomandibular disorder, including myofascial pain.

To the investigator's knowledge, no previous prospective, randomized study has been conducted demonstrating the treatment outcomes of either trigger point injections or twin block in patients with chronic myofascial pain.

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 (Participant, Care Provider)

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients diagnosed with Myofascial pain with referral based on the DC/TMD criteria
  • Pain on the masseter and or temporalis muscles
  • Pain present for at least 3 months

排除标准

  • Generalized muscle disorder such as fibromyalgia
  • Subjects on chronic pain medication
  • Subjects who are known to have hypersensitivity to the local anesthetics.
  • Pregnant women. A pregnancy test will not be given before subject enrollment. Women of childbearing ages will be asked verbally if they are pregnant. If they are unsure, then they will be excluded from the study.
  • Subjects with cognitive problems e.g. Alzheimer's disease.

结局指标

主要结局

Pain relief: numerical pain scale

时间窗: 6 months

The pain relief received from each injection will be measured using the numerical pain scale. This scale is between 0-10 with 0 meaning no pain and 10 is the most pain.Higher values represent worse pain.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sowmya Ananthan

Principal Investigator

Rutgers University

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