Changes of Acupoint Sensitization Characteristics on Gallbladder Meridian and Acupuncture Intervention Effect in Patients with Cervical Spondylosis
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Visual Analogue Scale
研究概览
简要总结
To investigate the changes of acupoint sensitization characteristics of patients with Neck Type Cervical Spondylopathy through Gallbladder meridian observe the curative effect of acupuncture intervention and optimize the clinical diagnosis and treatment plan of acupuncture treatment of Neck Type Cervical Spondylopathy
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 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Meeting the diagnostic criteria of Neck Type Cervical Spondylopathy.
- •Age 18 to 65 years old gender is not limited.
- •Clear awareness good compliance willing to cooperate with the study and accept the experimental arrangement.
- •Physical examination may or may not be accompanied by positive signs of the musculoskeletal system (including limited motor function local tender points etc.).
- •The visual analogue Scale (VAS) score was more than 3 points and less than 7 points (ranging from 0 to 10 points).
- •Informed consent and sign informed consent.
排除标准
- •It does not meet the diagnostic criteria and inclusion criteria of cervical spondylosis.
- •Under 18 years of age or over 65 years of age;
- •2 weeks before the start of the experiment the relevant treatment of the disease or the use of relevant therapeutic drugs;
- •Patients with other types of cervical spondylosis (cervical radiculopathy vertebral artery type cervical spondylosis cervical myelopathy sympathetic cervical spondylosis) or with other serious organic diseases and patients with neck and shoulder pain caused by non-neck diseases;
- •Patients with cardiovascular and cerebrovascular liver kidney digestive system blood system and other serious life-threatening primary diseases or suffering from hemorrhagic diseases or skin diseases or pregnant or lactating women or have a history of cardiac pacemaker implantation;
- •Previous history of neck surgery or neck fracture;
- •Persons with confusion mental disorder or cognitive impairment;
- •The skin at the test site has scars redness swelling heat and pain that affect the test result.
结局指标
主要结局
Visual Analogue Scale
时间窗: Before the start of treatment, immediately after the end of the third treatment, and four weeks after follow-up
The visual Analogue Scale (VAS) ranging from 0 to 10, with higher scores reflecting more pain, stiffness and poorer physical function of the Cervical. Participants were asked to evaluate their current pain, and the pain nature was marked by X on the line above. 0 was classified as painless and 10 was classified as severe pain. The higher the score, the more obvious the pain.
次要结局
- musculoskeletal ultrasound detection of cervical(Before the start of treatment, immediately after the end of the third treatment)
- Pressure pain threshold(Before the start of treatment, immediately after the end of the third treatment, and four weeks after follow-up)
- The Neck Disability Index(Before the start of treatment, immediately after the end of the third treatment, and four weeks after follow-up)
- Cervical range of motion scale(Before the start of treatment, immediately after the end of the third treatment, and four weeks after follow-up)
- The 12 items Short Form Health Survey(Before the start of treatment, immediately after the end of the third treatment, and four weeks after follow-up)
研究者
LiChaoran
Attending physician
The Third Affiliated hospital of Zhejiang Chinese Medical University