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临床试验/NCT00656110
NCT00656110Unknown不适用

Randomized, Placebo-Controlled Trial of Bilateral 3rd/4th Common Digital Foot Nerve Injections to Treat Restless Legs Syndrome

Lowcountry Infectious Diseases1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2008年4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
发起方
入组人数
60
试验地点
1
主要终点
International Restless Legs Rating Scale

研究概览

简要总结

The purpose of this study is to determine whether, in a randomized, placebo-controlled trial, restless legs syndrome (RLS) can be caused by pinched and damaged foot nerves called neuromas.

详细描述

Restless legs syndrome (RLS) is a medical condition in which there is an almost irresistible urge to move the legs in response to uncomfortable, difficult-to-describe leg sensations that are usually worse in the evening and especially noticeable when inactive such as sitting in a chair watching TV or when resting in bed trying to go to sleep or back to sleep after awakening. Most patients with RLS, while asleep, also have involuntary leg movements called periodic limb movements of sleep (PLMS). During a sleep study, brain wave monitoring of patients with RLS/PLMS often shows that the nighttime leg movements are associated with brain stimulation and arousal to a lighter stage of sleep. When many such brain arousals happen through the night, the natural pattern of deep sleep may be severely disrupted. Such disturbed sleep is of poorer quality and is less refreshing. The combination of RLS-related delay of initiation or resumption of sleep and PLMS-related poor quality of sleep may result in a severe sleep disorder manifested by morning sluggishness and increased daytime fatigue. The cause(s) of RLS and PLMS have not been determined. Neurologists believe that they originate in the brain in areas that control movement and may be related to localized low levels of dopamine (a chemical messenger between nerve cells) or related to disordered brain iron metabolism, but these theories have never been proven.

RLS and PLMS generally are lifelong conditions for which there is no cure. RLS is treated with medications targeting the brain and categories of drugs that have been used to treat symptoms (with varying success) include mainly dopaminergic drugs but also sedatives, anti-seizure drugs, and pain medications such as narcotics. Two dopaminergic drugs have been approved by the FDA for the treatment of RLS: ropinirole ("Requip") in 2005 and pramipexole ("Mirapex") in 2006. However such drugs are far from ideal because, in addition to the problem of side effects, some patients may not respond to these drugs or symptoms may only partially improve. Also, any improvement only occurs while continuing to take the drug, and finally, symptoms may sometimes become much worse after an initial period of improvement, a phenomenon called augmentation.

Foot neuromas are nerve entrapments ("pinched nerves") which form at points where the common interdigital nerves must stretch under ligaments between the metatarsal heads in the ball of each foot. Repeated irritation and damage to the nerves at those stretch points eventually results in fibrous thickening and enlargement of the nerve tissue into a lump called a neuroma. This most commonly involves a nerve in the ball of the foot between the third and fourth toes ("Morton's Neuroma"), but neuromas also often form at the entrapment/stretch point of the nerves between the second/third and fourth/fifth toes.

Neuromas may be completely asymptomatic in the foot or may cause variable degrees of unilateral or bilateral foot pain and numbness brought on or made worse by tight shoes, high heels, or prolonged walking or standing. When neuromas become more severely symptomatic, they may cause neuropathic symptoms such as burning, tingling, numbness, electric shock shooting pains, and hypersensitivity. Neuromas are treated with a series of injections (local anesthetic combined with either steroids and/or alcohol solution) given into the neuroma-containing space in the ball of the foot. It is believed that these injections serve to calm the nerve irritability which usually results in improvement or sometimes even complete resolution of the neuropathic symptoms (burning pain, etc.).

Previous studies by our group determined that many patients with neuropathic foot symptoms (burning, tingling, electric shocks, numbness, etc.) who had been previously diagnosed with "peripheral neuropathy," actually had neuromas in both feet as the cause of their symptoms. The causative role of neuromas in these patients was demonstrated by the fact that their chronic pain symptoms improved (in some cases markedly so) with standard neuroma injection treatment. In addition to improvement in their neuropathic foot pains, many patients also reported that they were sleeping much better. Such patients reported not only a decrease in their RLS-type leg restlessness but also that their spouse had noted a decrease in their PLMS-type nighttime leg movements, all as a direct result of their bilateral neuroma injections. These reports prompted further study of patients who had RLS/PLMS both with and without neuropathic foot pains.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Clinical symptoms (that fulfill the 4 essential clinical criteria for RLS) of at least 6 months duration with a current IRLS-rs score indicative of at least moderate severity (15 or greater)
  • Evidence of bilateral 3rd/4th interspace neuromas by both physical examination and ultrasound criteria at initial evaluation
  • Willingness and ability of patient to participate in initial weekly evaluation/neuroma treatment visits and subsequent periodic follow-up visits over a period of approximately 6-9 weeks.
  • Off dopaminergic drug treatment (ropinirole-"Requip" or pramipexole-"Mirapex") starting 2 weeks prior to the initial foot injections and for the duration of the study.

排除标准

  • Major foot deformity, previous major foot surgery, or previous neuroma injections
  • Known or suspected obstructive sleep apnea
  • Allergy to any of injection components (depo-medrol, lidocaine, marcaine, absolute alcohol)
  • Pregnancy

研究组 & 干预措施

1-T

Experimental

Treatment Group

干预措施: equal parts of 0.5% plain Marcaine and 2% lidocaine mixed with 0.8 mg Depo-medrol/4% absolute alcohol in a total injection volume of 1 ml (Drug)

2-P

Placebo Comparator

Placebo comparator

干预措施: Normal saline - 1ml (Drug)

结局指标

主要结局

International Restless Legs Rating Scale

时间窗: Weekly during the study and three weeks after treatment completion

次要结局

未报告次要终点

研究者

发起方
Lowcountry Infectious Diseases
申办方类型
Other

研究点 (1)

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