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Observation on the Curative Effect of Acupuncture At Sensitized Points on Gallbladder Meridian in the Treatment of Neck Type Cervical Spondylopathy

L

LiChaoran

Status

Not yet enrolling

Conditions

Cervical Spondylopathy

Treatments

Procedure: Sham acupuncture
Procedure: Acupuncture

Study type

Interventional

Funder types

Other

Identifiers

NCT06847945
ZSLL-KY-2023-040-03

Details and patient eligibility

About

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

Enrollment

80 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

80 participants in 2 patient groups

Non-meridian,non-acupoint group
Sham Comparator group
Treatment:
Procedure: Sham acupuncture
Acupoint sensitization group
Experimental group
Treatment:
Procedure: Acupuncture

Trial contacts and locations

1

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Central trial contact

Chaoran Li

Data sourced from clinicaltrials.gov

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