NCT07445191尚未招募2 期
Clinical Assessment of The Efficacy of Triamcinolone-Lidocaine Mix in Trigger Points Injection of Masseter Muscle: Double-blinded, Randomized Controlled Trial
干预措施
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 入组人数
- 30
- 主要终点
- current pain intensity
研究概览
简要总结
This study aims to clinically evaluate the efficacy of trigger points using active drug mix (Triamcinolone with lidocaine) on relief of myofascial pain of jaw muscle.
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, Care Provider, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age more than or equal 18 years
- •Patients' willingness to follow instructions
排除标准
- •Patients who will be using any medications to reduce the pain and/or have any effect on the skeletal muscle
- •Clinical conditions such as pregnancy
- •Medical problems that may interfere with the procedures such as bleeding disorders
- •Cognitive impairment or exhibited inadequate cooperation
- •Patients will be receiving physical therapy or wearing occlusal splint in the same period of the research
研究组 & 干预措施
Saline
Active Comparator
干预措施: Saline (Drug)
Triamcinolone with lidocaine
Experimental
干预措施: Triamcinolone with lidocaine (Drug)
Lidocaine
Experimental
干预措施: Lidocaine (Drug)
结局指标
主要结局
current pain intensity
时间窗: 1 week , 1 month , 3 months after treatment
• Patients' subjective pain experience. Each patient will be asked to rate his or her current and worst pain intensity on visual analogue scale (VAS) of 0-10 with zero being no pain and ten corresponds to the worst pain that the patient ever had
次要结局
- post operative demands for analgesics(1 week , 1 month , 3 months after treatment)
- patient satisfaction(1 week , 1 month , 3 months after treatment)
- maximum mouth opening(1 week , 1 month , 3 months after treatment)
- pressure pain threshold (PPT)(1 week , 1 month , 3 months after treatment)
研究者
Ammar Ali Mudhsh Al hawbani
AAMAHawbani
Cairo University
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