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临床试验/NCT06824324
NCT06824324已完成1 期

Is Botulinum Toxin Predictable in the Management of Myofascial Pain Syndrome Related to Masticatory Muscles?

Yassir R. Al-khannaq1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2024年3月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
14
试验地点
1
主要终点
Pain level

研究概览

简要总结

The objective of this study was to assess the efficacy of Botulinum toxin type (A) (BoNTA) injection in Myofascial pain syndrome management in the terms of duration of function improvement and pain reduction.

Material and methods: Fourteen patients with Myofascial pain syndrome related to masticatory muscles were presented with trismus, pain and impairment of oral function. Treatment plan was established by utilizing thirty units of Botulinum toxin type (A) which was injected into masseter and sometimes temporalis muscle.

详细描述

Myofascial pain syndrome (MPS) is acute or chronic musculoskeletal pain that characterized by the presence of unique trigger points of pain (TrPs) . Etiology of this condition may include psychogenic stress, prolong muscle strain, trauma to the joint or muscle, arthritis, myositis, chronic infection, and general fatigue. Current therapeutic approaches available for Myofascial pain syndrome involved pharmacological and non-pharmacological treatment options. The non-pharmacological techniques may include a) manual therapy by muscle stretch or massage, b) muscular taut band injection by local anesthesia or botulinum toxin, c) acupuncture, and d) therapeutic ultrasound .

Botulinum toxin is a neurotoxin protein produced by anaerobic bacteria (clostridium botulinum) . It was first discovered by a German physician named Justinus Kerner who observed that the toxin acts by impeding signal transmission in the somatic and autonomic motor systems, leaving the sensory signal transmission uninterrupted .

It blocked the acetylcholine release from the nerve endings thus prevent the neurological signals transmission at the neuromuscular junction. In turn, this reduces the muscle contraction and produces relaxation of the muscle . However, the clinical effects of Botulinum toxin are transit as these neurotoxins degenerate at nerve terminals and became inefficient after a period of time .

Although numerous articles were published on the Botulinum Toxin A (BoNTA) injection in the management of MPS, but there were diverse clinical results in the literature regarding this subject and its effectiveness is still questionable . The objective of this study was to evaluate the efficiency and outcomes of BoNTA injection in the management of MPS related to masticatory muscles.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patient with myofascial pain related to the muscles of mastication (masseter and temporalis muscle).
  • •Patient with regional pain.
  • •Patient with or without limited mouth opening (trismus).
  • •Presence of trigger points within the identified masticatory muscles.

排除标准

  • •Hypersensitivity to Botulinum toxin.
  • •Active infection in the virtual points of injection.
  • •Patient with generalized musculoskeletal pain as in Fibromyalgia Syndrome (FMS).
  • •Children younger than 12 years old and pregnant woman. 5-Patient recently undergone to one other modality of treatment

研究组 & 干预措施

injection of Botulinum toxin A in Triger zone

Active Comparator

The method utilized for dilution of Botulinum toxin A involved addition of 2.5ml of normal saline to 100 unit of Botox vial, and addition of 1.25ml to 50U of Botox so each 0.1ml contain 4U of Botox.

Botox can be denatured easily so the dilution process was very precise and the dilute injected gently in to Botox Vial.

A thirty units of Botulinum toxin A was injected intramuscularly bilaterally (30 U for each side) in thirteen patients and unilaterally in one patient

干预措施: intramuscular Botulinum Toxin (Drug)

结局指标

主要结局

Pain level

时间窗: 16 weeks

Pain level was assessed before the initiation of treatment and at 2, 8 and 16 weeks after injection by using the visual analogue scale

次要结局

  • Mouth opening(16 weeks)

研究者

发起方
Yassir R. Al-khannaq
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Yassir R. Al-khannaq

LECTURER Dr.

University of Baghdad

研究点 (1)

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