跳至主要内容
临床试验/NCT00991848
NCT00991848已完成1 期

Effect of Intravenous Lidocaine on Manifestations of Fibromyalgia

Federal University of São Paulo1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2005年1月最近更新:
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
30
试验地点
1
主要终点
effect of the combination of intravenous lidocaine and amitriptyline on the clinical manifestations of fibromyalgia

研究概览

简要总结

Background and Objectives: Fibromyalgia is a pain syndrome characterized by numerous manifestations. The objective of this study was to evaluate the effect of the combination of intravenous lidocaine and amitriptyline on the manifestations of fibromyalgia. Methods: A prospective, randomized, double-blind, comparative study was conducted. All patient received 25 mg amitriptyline. Patients of group 1 (n = 15) received 125 mL 0.9% saline, and patients of group 2 (n = 15) received 240 mg lidocaine in 125 mL 0.9% saline once a week for 4 weeks. Manifestations were recorded before and 4 weeks after treatment. Pain intensity was rated on a verbal numerical scale.

详细描述

Amitriptyline was chosen in the present study because it is the most widely used antidepressant with proven analgesic efficacy for the treatment of a variety of chronic pain syndromes. Amitriptyline also promotes improvement of sleep, an effect observed in the present study.

Lidocaine has been widely applied by the intravenous route and patients with a variety of pain syndromes, including fibromyalgia, have reported pain relief with this technique.The dose of lidocaine employed by various investigators ranges from 1 to 5 mg/kg administered over a period of 30-60 min. The minimum effective dose is 1.5 mL/L, which is achieved with 2-5 mg/kg infused over 30-60 min. In these study, 240 mg lidocaine was administered, corresponding to about 3 mg/kg.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • pain in the four quadrants of the body for at least 3 months
  • sleep disorders
  • subjective edema
  • depression
  • paresthesia.

排除标准

  • alterations in thyroid
  • rheumatological
  • renal and hepatic function
  • rheumatic, neuromuscular or psychiatric disease
  • infectious arthropathy
  • other pain syndromes
  • drug hypersensitivity
  • pregnancy

研究组 & 干预措施

Lidocaine

Experimental

Patients received 240 mg lidocaine diluted in 125 mL 0.9% saline. The solutions were infused over a period of 1 h, once a week, for 4 weeks (T1, T2, T3 and T4).

干预措施: Lidocaine (Drug)

结局指标

主要结局

effect of the combination of intravenous lidocaine and amitriptyline on the clinical manifestations of fibromyalgia

时间窗: 4 weeks

次要结局

  • Pain intensity by numerical scale (0 - 10)where 0 being an absent of pain and 10 measuring as the highest for pain intensity(4 weeks)

研究者

发起方
Federal University of São Paulo
申办方类型
Other

研究点 (1)

Loading locations...

相似试验