CTRI/2024/05/067131招募中4 期
Efficacy of transdermal diclofenac patches in management of pain associated with Myofascial pain dysfunction syndrome
Harshini M1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年5月20日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Reduction in pain will be assessed using Visual analog score
研究概览
简要总结
Transdermal diclofenac patches are as effective as oral diclofenac in management of pain associated with myofascial pain dysfunction syndrome.So,the aim of the study is to evaluate the reduction in pain score with oral and transdermal diclofenac patches and compare their efficacy in management of pain associated with Myofascial pain dysfunction syndrome.
研究设计
- 研究类型
- Interventional
- 分配方式
- Stratified randomization
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •1.Patients who were clinically diagnosed with MPDS according to Laskin’s criteria 2.Systemically healthy individuals 3.Patients who are conscious and co-operative and are able to give the Visual Analog Score (VAS).
排除标准
- •Patients with: 1.Missing teeth 2.Grossly decayed teeth 3.Allergy to diclofenac or any other NSAIDs 4.Any systemic and connective tissue disorders 5.Undergoing treatment with other NSAIDs or any other analgesics during the study period 6.Gastritis 7.Pregnant women 8.Trauma/Malignancy of the maxillofacial region.
结局指标
主要结局
Reduction in pain will be assessed using Visual analog score
时间窗: Reduction in pain will be assessed using Visual analog score at baseline and 7th day after intervention
次要结局
- Efficacy in Management of pain(Reduction in pain score will be assessed for determining the efficacy at baseline & 7th day)
研究者
研究点 (1)
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