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临床试验/NCT01304082
NCT01304082终止不适用

A Single-center, Randomized, Double-blind Clinical Study to Evaluate the Effect of pH on Pain Upon Local Anesthetic Administration.

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2011年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
29
试验地点
1
主要终点
Rank-transformed Pain Score

研究概览

简要总结

When one receives a local anesthetic, such as novocaine for a dental procedure, there is a burning painful sensation experienced upon injection of the local anesthetic. We are trying to understand the role of pH (how acidic a solution is) in the production of pain during local anesthetic administration. We hypothesize that less acidic solutions produce less burning. We also want to determine whether or not the pH of the solution affects the rate of onset of the local anesthesia. We will recruit subjects from patients who have a clinical indication for lumbar medial branch (LMB) nerve blocks, procedures frequently performed at the Massachusetts General Hospital Center for Pain Medicine. For each patient, three nerve blocks are administered at adjacent spinal levels, typically using either lidocaine or bicarbonate-buffered lidocaine as the local anesthetic. We will add a saline control as part of the research procedure and then provide lidocaine at the control location before continuing with the nerve blocks. This clinical procedure offers an ideal opportunity to compare the effects of the three solutions. There will be almost no deviation from the standard clinical procedure. After the injection of each solution, the pain score on administration of the medication will be recorded immediately. We will also provide a continuous stimulation (pin taps) after the local anesthetic injection and record when the patient experiences hypoesthesia (reduced sensation) and anesthesia (absent sensation). Finally, we will record the pain score upon reinsertion of a needle to mark the precise location (part of the clinical procedure) one minute after the local anesthetic injection. All data will be collected during the a single clinical visit.

The study will conclude when 60 subjects have successfully been tested. Data will be reviewed annually.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients at MGH Center for Pain Medicine who have clinical indication for undergoing diagnostic medial branch block of nerves to facet joints.

排除标准

  • contraindication to the clinical procedure
  • do not speak English

研究组 & 干预措施

normal saline

Placebo Comparator

干预措施: normal saline (Drug)

lidocaine

Active Comparator

干预措施: Lidocaine (Drug)

alkalinized lidocaine

Experimental

干预措施: alkalinized lidocaine (Drug)

结局指标

主要结局

Rank-transformed Pain Score

时间窗: immediate, upon injection of each solution

Pain score upon injection of local anesthetic: the pain score is a validated 11-point numeric rating scale in which patients rate pain between 0 (no pain) and 10 (worst pain imaginable).

次要结局

  • Rank-transformed Time (Seconds) Until Anesthesia(0-180 seconds after each injection)
  • Rank-transformed Pain Score Upon Needle Stick.(1 minute after each injection)
  • Rank-transformed Time (Seconds) Until Hypoesthesia(0-180 seconds after each injection.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Brian Wainger

Instructor

Massachusetts General Hospital

研究点 (1)

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