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Clinical observation of different acupoint prescriptions in the treatment of neck pain caused by cervical spondylosis in qi stagnation and blood stasis type

Phase 1
Recruiting
Conditions
cervical spondylosis
Registration Number
ITMCTR1900002543
Lead Sponsor
Shanghai Shuguang Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1) accord with the diagnostic criteria for cervical spondylosis;
2) caused by neck trauma or injury, stiff and pain neck with fixed pain points, the pain will intensified when move; often accompanied by limb numbness, pale red tongue with purple dark spots (or not), string or uneven pulse
3) Aged 18 to 65 years;
4) The course of neck pain >=12 weeks;
5)VAS 3 to 7 before treatment;
6) Have not taken any painkillers or glucocorticoids in the past 2 weeks;
7) Sign the informed consent form, volunteer to participate and cooperate with the researcher.

Exclusion Criteria

1) Those who do not accord with the above inclusion criteria;
2) pregnant or lactating women;
3) cervical spondylotic myelopathy, or other indications for absolute surgery, must be treated surgically;
4) Those who have serious diseases such as cardiovascular, cerebrovascular, liver, kidney, hematopoietic, digestive system, or mental illness;
5) Have received cervical spondylosis-related treatment within 1 month, or have received other treatments that may affect the effector indicators of the study;
6) Can not correctly understand and fill out the various scales related to the research;
7) Reluctant to join the tester;
8) The investigator believes that it is not appropriate to participate in other situations in this study.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
vas;
Secondary Outcome Measures
NameTimeMethod
SF-36;FDIX Force One;NDI;NPQ;
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