Clinical study on the treatment of cervical spondylosis by
- Conditions
- Cervical spondylosis
- Registration Number
- ITMCTR2200006850
- Lead Sponsor
- Affiliated Hospital of Nanjing University of Chinese Medicine (Jiangsu Hospital of Traditional Chinese Medicine)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
2.1 In line with Western medicine diagnostic standards for cervical spondylosis, X-ray, CT, MRI and other imaging data of cervical vertebra open mouth were complete;
2.2 Age range from 20 to 70;
2.3 A washout period of more than 5 days for patients with cervical spondylosis who have received other treatments;
2.4 Willing to accept TCM bone-setting treatment;
2.5 Good compliance, signed informed consent to ensure that the implementation of the program during the test;
2.6 The oral radiographs of the patient's cervical spine indicated that the atlantodental space gap was greater than 0.5MM.
3.1 Cervical spondylotic radiculopathy with surgical indications shall be excluded. ?
3.2 Patients with systemic bone and joint diseases, cervical tumor and tuberculosis, severe cervical trauma or cervical surgery history that may affect the results of the study;
3.3 Patients with vertebral artery cervical vertigo attack who could not take care of themselves;
3.4 Complicated with serious primary diseases of heart, cerebrovascular, liver, kidney, hematopoietic system, endocrine system and mental disorders;
3.5 The injured skin is damaged, or other diseases affect the injured local massage treatment, such as skin diseases;
3.6 Women who are breastfeeding, pregnant or preparing to become pregnant;
3.7 Patients who are participating in clinical trials of other drugs;
3.8 In addition to cervical spondylosis, pain relievers (such as acetaminophen, non-steroidal anti-inflammatory drugs, compound over-the-counter drugs containing analgesic ingredients, Chinese medicines that may contain analgesic active ingredients, local pain relievers) are needed for other chronic or recurrent pain;
3.9 Other diseases or conditions that could reduce or complicate enrollment, such as frequent changes in the working environment, could easily cause loss of follow-up as determined by the investigator.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method eck Disfunction Index;fMRI;
- Secondary Outcome Measures
Name Time Method Cervical Range of Motion;Visual Analog Scales;