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Clinical study on the treatment of cervical spondylosis by

Clinical study on the treatment of cervical spondylosis by

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006850
Enrollment
Unknown
Registered
2022-12-02
Start date
2022-12-10
Completion date
Unknown
Last updated
2023-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical spondylosis

Interventions

control group:Traditional massage therapy
treatment group:TCM bone-setting massage therapy

Sponsors

Affiliated Hospital of Nanjing University of Chinese Medicine (Jiangsu Hospital of Traditional Chinese Medicine)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

MeasureTime frame
Neck Disfunction Index;fMRI;

Secondary

MeasureTime frame
Cervical Range of Motion;Visual Analog Scales;

Countries

China

Contacts

Public Contactsongshilong
ssl19841128@163.com18751976688

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026