Observation on the Curative Effect of Acupuncture At Sensitized Points on Gallbladder Meridian in the Treatment of Neck Type Cervical Spondylopathy
NCT ID: NCT06847945
Last Updated: 2025-02-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
80 participants
INTERVENTIONAL
2025-03-05
2025-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Non-meridian，non-acupoint group
Sham acupuncture
Patients in the non-meridian and non-acupoint group received sham acupuncture treatment at the position 2cm apart from the sensitized acupoint, once every other day for 30min each time, a total of 3 times for 1 week.
Acupoint sensitization group
Acupuncture
Patients in acupoint sensitization group were treated with pseudoacupuncture at the sensitized points once every other day for 30min each time, a total of 3 times for 1 week.
Interventions
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Sham acupuncture
Patients in the non-meridian and non-acupoint group received sham acupuncture treatment at the position 2cm apart from the sensitized acupoint, once every other day for 30min each time, a total of 3 times for 1 week.
Acupuncture
Patients in acupoint sensitization group were treated with pseudoacupuncture at the sensitized points once every other day for 30min each time, a total of 3 times for 1 week.
Eligibility Criteria
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Inclusion Criteria
* 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.
* 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.
18 Years
65 Years
ALL
No
Sponsors
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LiChaoran
OTHER
Responsible Party
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LiChaoran
Attending physician
Principal Investigators
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Chaoran Li
Role: STUDY_CHAIR
The Third Affiliated hospital of Zhejiang Chinese Medical University
Locations
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The Third Affiliated Hospital of Zhejiang Chinese Medicine University
Hangzhou, , China
Countries
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Central Contacts
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Facility Contacts
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Role: primary
Other Identifiers
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ZSLL-KY-2023-040-03
Identifier Type: -
Identifier Source: org_study_id
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