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临床试验/NCT06814535
NCT06814535进行中(未招募)2 期

A Comparative Study on the Impact of Trigger Points Injection of Platelet Rich Plasma Versus Botulinum Toxin a on the Relief of Jaw Muscles Myofascial Pain

Cairo University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
进行中(未招募)
入组人数
60
试验地点
1
主要终点
Pressure pain threshold

研究概览

简要总结

This study aims at comparing the effect of trigger points injection of platelet rich plasma and botulinum toxin a on the relief of jaw muscles Myofascial pain .

The 1st group includes 20 patients who are supposed to receive 5 units of botulinum toxin A per trigger point in masseter and/or temporalis muscles.

The 2nd group will receive ,5 ml of PRP per trigger point in masseter and/or temporalis muscles.

The 3rd group will receive .5 ml of physiologic saline per each trigger point in masseter and/or temporalis muscles.

The 1st follow up session will be after 1 week then 1 month then 3 months . The patients are advised to limit excessive Mouth opening, yawning or singing. And when pain episode , theta re advised to take only paracetamol as analgesic drug .

At the follow up sessions ، measuring the interincisal opening , pressure pain threshold using algometer , VAS to measure the intensity of pain , Likert scale , current pain intensity, worst pain intensity and the need to take analgesics in Numbers.

Then comparing the results of these groups to end in rejecting the null hypothesis which says there's an equivalence between the 3 types of injected solutions or accepting it .

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
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •patient with myofascial trigger points in masseter or temporalis previously ----*identified by manual palpation.
  • •18 years or More "Willingness to follow instructions.

排除标准

  • •therapeutic intervention for myofascial pain in the last view months such as taking medications for pain control or wearing an occlusal splint.
  • •Clinical conditions as pregnancy
  • •Medical problems that will interfere with the procedure as bleeding disorders.
  • •Cognitive impairment or present inadequate cooperation.

研究组 & 干预措施

Botulinum toxin A

Active Comparator

20 Patients with Myofascial pain will be injected by 5 units botulinum toxin A per trigger point in masseter and/or temporalis

干预措施: Botulinum Toxin A / Botulinum Toxin A (Drug)

结局指标

主要结局

Pressure pain threshold

时间窗: 3 months

The amount of force per kilogram needed to induce pain in patients with myofascial pain at the trigger point.. Will be measured using the algometer which presses on the trigger point to induce pain by force measured in kilograms/cm2 If the reading increased among the treatment visits , this means better outcome and decreased pain intensity with effectiveness of the treatment

Current pain intensity

时间窗: 3 months

The amount of pain on VAS at the time of examination from 0-10 With 0 no pain which increases to reach 10 ( the highest pain intensity).. Decrease in pain intensity means better outcome

Worst pain intensity

时间窗: 3 months

The worst pain the patient had suffered from on the previous duration. Using visual analogue scale from (0-10) with 0 least pain and 10 worst pain . Decrease in pain intensity means better outcome

次要结局

  • Inter incisal opening(3 months)
  • Patient satisfaction(3 months)
  • The need for analgesics(3 months)

研究者

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

asmaa abdelrahman abdelhakeem sayed

Principal investigator

Cairo University

研究点 (1)

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