Evaluation of effect of sedation on diagnostic cervical facet joint nerve blocks

Ambulatory Surgery Center and Pain Management Center of Paducah (USA)0 个研究点目标入组 180 人开始时间: 2005年11月17日最近更新: 2015年1月13日

适应症

试验速览

暂无简介。

•1. Subjects were between 18 and 90 years of age
•2. Subjects had a history of chronic, function limiting, neck pain of at least 6 months duration
•3. Subjects were able to give voluntary, written informed consent to participate in the investigation
•4. Subjects who, in the opinion of the investigator, are able to understand the investigation, and/or cooperate with the investigational procedures
•5. Subjects who had undergone diagnostic facet joint blocks and the diagnosis of cervical facet joint pain has been confirmed previously

•1. Subjects without cervical facet joint pain
•2. Subjects with uncontrollable major depression or uncontrolled psychiatric disorders
•3. Pregnant or lactating women
•4. Subjects with multiple complaints involving multiple other problems with overlapping pain complaints
•5. Subjects unable to achieve appropriate positioning and inability to understand informed consent and protocol
•6. Subjects with a history of adverse reaction to either midazolam or fentanyl

发起方

Ambulatory Surgery Center and Pain Management Center of Paducah (USA)