NCT01381380已完成不适用
Effect of Manual Therapy After Trigger Point Injection for Myofascial Pain Syndrome
Federal University of São Paulo2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2006年11月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 30
- 试验地点
- 2
- 主要终点
- Pain intensity
研究概览
简要总结
This study is a pain intensity evaluation in patients with myofascial pain submitted kinesitherapy after trigger point injection.
详细描述
Randomized prospective study conducted on 30 patients of both genders ranging in age from 18 to 60 years, with neck and shoulder girdle Myofascial Pain Syndrome (MFS), with a duration of ≥ 4 months and pain intensity ≥ 4.
Trigger point injection of 1 mL 0.25% bupivacaine at each point, once a week for 8 weeks (T1 to T8).
Group 1: kinesiotherapy once a week for 8 weeks Group 2: not submitted to kinesiotherapy Evaluation of pain intensity on the first assessment (T0) and after 1, 2, 3, 4, 5, 6, 7, 8, and 9 weeks
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •myofascial pain of neck and shoulder girdle, lasting ≥ 4 months, pain intensity ≥ 4.
排除标准
- •arrhythmia
- •heart block
- •coagulopathy
- •cognitive alterations and infection at the site
- •patients using anticoagulants, and pregnant women
结局指标
主要结局
Pain intensity
时间窗: 8 weeks
once a week for 8 weeks (T1 to T8)
次要结局
未报告次要终点
研究者
研究点 (2)
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