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临床试验/NCT05053984
NCT05053984Unknown不适用

Ultrasound-Guided Percutaneous Neuromodulation in Spasticity

Hospital Universitario de Canarias2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2021年11月2日最近更新:
适应症

试验速览

阶段
不适用
入组人数
30
试验地点
2
主要终点
Spasticity

研究概览

简要总结

The Multiple sclerosis (MS) is a chronic, inflammatory, autoimmune disease characterised by the appearance of lesions, characterised by heterogeneity in their anatomopathological, clinical and radiological presentation.

Its aetiology is complex and multifactorial, with genetic and environmental interactions with a predominance in women (3:1) and is the second leading cause of disability in young adults (25-30 years). It has a socio-economic impact, affecting interpersonal relationships and causing a significant reduction in quality of life.

MAIN OBJECTIVE To assess the effect on spasticity of the Percutaneous Ultrasound-guided Neuromodulation (PMN) technique in patients diagnosed with MS with upper limb spasticity.

SECONDARY OBJECTIVES

  • To assess changes in the strength parameter of the wrist flexor musculature wrist before and after the application of a PMN programme.
  • To assess changes in the functionality scales (modified Asworth, established for spasticity
  • To assess changes in the range of motion (ROM) of the joints under study.
  • Assess changes in the quality of life scale (MSQOL54).
  • To assess the adverse effects of the technique.

All patients will receive a Percutaneous Echoguided Neuromodulation (PNM) in the median nerve at the elbow, medial to the brachial artery, running between the humeral and ulnar heads of the pronator teres muscle. Once the nerve is located, a needle shall be inserted in the vicinity of the nerve and is stimulated using an electrical current with a frequency of 10 Hz, with a pulse width of 250 µs and a tolerable intensity causing a visible muscle cont raction for 1.5 minutes.

After assessing the correct application of ethics in the study, it was decided to use the individual's own baseline data as a control group, as simulating the technique is complex.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Sign the consent form to participate in the study
  • Be a patient diagnosed with Multiple Sclerosis.
  • Be over 18 years of age and less than or equal to 55 years of age.
  • Have spasticity (Asworth 2) in the upper limb.
  • Be able to travel to the place of the session

排除标准

  • Failure to comply with the above
  • Withdrawal of informed consent
  • Having a disease associated with MS that is incompatible with the technique. Use of anticoagulation
  • Cognitive impairment
  • Belenophobia

结局指标

主要结局

Spasticity

时间窗: 8 weeks

Modified Ashworth Scale which is a measure for the quantification of hypertonia of any articulation. It is a qualitative exam, with values in a range 0 to 4.

9 hole peg test

时间窗: 8 weeks

9HP: Test to assess limb function upper / hand. The patient is asked to incorporate 9 pins into a board with 9 holes, one in each hole, as fast as they can using their dominant hand. Once the test is done, it is repeated one more time for each hand.

Patient's quality of life

时间窗: 8 weeks

MSQOL 54: It's a questionnaire that measure mental and physical aspects. The range is from 0 to 100, where 100 is the highest grade of quality of life

Patient Functionality

时间窗: 8 weeks

Barthel Index: It's a measure of physical disability which assess functional disability in the activities of the daily life (ADL). The global range can vary between 0 (completely dependent) and 100 points (completely independent)

Muscle strength

时间窗: 8 weeks

Dynamometer: Dynamometry is an objective way of measuring muscle strength performed by an individual, managing to express it as a quantitative variable, which facilitates its assessment.

Range of Motion

时间窗: 8 weeks

Goniometer: Is used to assess changes in the range of motion (ROM) of the joints. The measurements made can be influenced by different factors: the ability to locate appropriate anatomical landmarks, evaluator experience, sex, weight, and age of the subject, as well as the type of joint. the level of reliability in the scan is somewhat greater in the joints of the upper limb than in the lower limb and this rises when more measurements are taken by the same examiner and on the same day.

Satisfaction Scale

时间窗: Immediately after the treatment

EVA Scale: It is an instrument for measuring subjective characteristics or attitudes that cannot be measured directly. Range:1-10

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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