跳至主要内容
临床试验/NCT01632215
NCT01632215已完成3 期

Effect of Preoperative Gabapentine for Carpal Tunnel Syndrome

Federal University of São Paulo0 个研究点目标入组 40 人开始时间: 2010年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
40
主要终点
Pain Intensity

研究概览

简要总结

The purpose of this study was to evaluate the postoperative analgesic effect of preoperative gabapentine for carpal tunnel syndrome surgery.

详细描述

There was studied 40 patients. Group 1 patients received 600 mg of gabapentin 1 hour before surgery; G2 received placebo 1 hour before surgery.

Anesthesia was regional intravenous block. Postoperative analgesia when needed was with acetaminophen. If needed was administered codeine. The evaluation of neuropathic pain was made by DN4 questionnaire. Pain intensity was assessed by numeric scale at block and after 30min, 1h, 2h, 2wk, 4wk, 6m. It was noted the duration of analgesia, and the amount of acetaminophen and codeine.

The statistical program used for analysis of the results was the Instat Graph

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, Investigator, 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

入选标准

  • carpal tunnel syndrome

排除标准

  • disorientation, psychiatric disease, myocardial ischemia, hypertension, arrhythmia, another pain syndrome, drug user, and pregnant

研究组 & 干预措施

sugar pill

Placebo Comparator

Placebo group

干预措施: Sugar pill (Other)

preoperative gabapentine,

Experimental

Gabapentine

干预措施: Gabapentine (Drug)

结局指标

主要结局

Pain Intensity

时间窗: 6 months

Numerical score from 0 to 10; zero means no pain and 10 is the more intense pain

次要结局

  • Chronic Pain(6 months)

研究者

发起方
Federal University of São Paulo
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rioko Kimiko Sakata

Pain Clinic Director

Federal University of São Paulo

相似试验