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A randomized controlled trial for efficacy and safety of Shi's manipulation in the treatment of acute and subacute neck pain

A randomized controlled trial for efficacy and safety of Shi's manipulation in the treatment of acute and subacute neck pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021371
Enrollment
Unknown
Registered
2019-02-17
Start date
2019-05-01
Completion date
Unknown
Last updated
2019-02-18

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

Conditions

Acute and Subacute Neck Pain

Interventions

Trial Group:Shi's manipulation
Controlled Group:Diclofenac Sodium Orally

Sponsors

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years; 2. Those who meet the above diagnostic criteria for acute and subacute neck pain; 3. VAS score of neck pain was 3 or more; 4. Those who volunteer to join the test and sign a letter of consent.

Exclusion criteria

Exclusion criteria: 1. Cervical spine fracture or dislocation; 2. Cervical spine, cervical soft tissue, cervical spinal cord tumors, tuberculosis; 3. Cervical spine fusion, paravertebral bridge and severe osteoporosis; 4. Cervical spine patients with surgical history; 5. The cervical spine or neck has a history of severe trauma; 6. There are skin inflammation and skin breakage in the neck; 7. Have serious heart, liver, kidney and hematopoietic system, peptic ulcer or bleeding, black stool and other diseases, mental patients; 8. Extremely deficient patients and pregnant women; 9. Those who participated in clinical trials of other drugs and treatments in the past three months had interference with this study; 10. Level II or IV in line with the Classification of Neck Pain and Related Diseases in the Ten-Year Strategic Task 2000-2010 of Bone and Joint: Grade III: No major structural and pathological changes occurred, but there were neurological signs such as weakened deep tendon reflex, decreased muscle strength, and/or loss of sensitivity, which may require further examination and invasive treatment if necessary. Class IV: Symptoms and signs of major structural and pathological changes, such as fractures, myelopathy, tumors, or systemic diseases, need prompt examination and treatment.

Design outcomes

Primary

MeasureTime frame
VAS score of neck pain;

Secondary

MeasureTime frame
Cervical vertebral dysfunction index;Measurement of cervical mobility;Improvement of patients'quality of life;

Countries

China

Contacts

Public ContactMingcai Zhang

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

zhangmc816@126.com+86 13524428805

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 24, 2026