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clinical study of cervical curvature rehabilitation device combined with joint loosening manipulation to correct abnormal cervical curvature

clinical study of cervical curvature rehabilitation device combined with joint loosening manipulation to correct abnormal cervical curvature

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035834
Enrollment
Unknown
Registered
2020-08-18
Start date
2021-01-01
Completion date
Unknown
Last updated
2020-08-24

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

Conditions

Abnormal cervical curvature

Interventions

Sponsors

Longhua Hospital, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Informed consent and sign informed consent form; 2. According to the diagnostic criteria of cervical spondylosis and abnormal cervical curvature; 3. Male or female aged 15-40 years; 4. Voluntarily accept the required joint loosening manipulation combined with cervical curvature rehabilitation appliance exercise; 5. No other treatment was given during the study period.

Exclusion criteria

Exclusion criteria: 1. The patients who refused the treatment plan randomly divided into two groups, and those who had participated in or were participating in other clinical researches in the past three months; 2. The muscle strength decreased significantly in a short period of time, and the muscle strength was lower than grade III. The patients who had been treated with regular non-surgical therapy for six months had no effect; 3. Patients with severe cervical pain, cervical spinal cord compression, cauda equina syndrome and unstable lower limb walking were found; 4. The patients with serious cervical deformity, fracture, osteopathy, tuberculosis, tumor and other complicated diseases by imaging examination, and those with severe cervical trauma history and cervical spondylosis surgery treatment history; 5. Patients with severe primary diseases such as liver, kidney, hematopoietic system, endocrine system, cardio cerebrovascular system, nervous system, tuberculosis, vertebral malformation, malignant tumor and psychosis; patients suspected of sedative hypnotics, opioid analgesics and alcohol abuse; patients with skin diseases and infectious diseases; patients with severe primary diseases such as liver, kidney, hematopoiesis, endocrine system, cardiovascular and cerebrovascular diseases, and psychiatric patients; 6. Pregnant woman, or ready for pregnancy or lactation; 7. Patients who are not suitable or unable to use this treatment method for other reasons; 8. Patients with mental disorders, language disorders, motor dysfunction, mental illness.

Design outcomes

Primary

MeasureTime frame
VAS score;NDI score;X-ray;

Countries

China

Contacts

Public ContactYe Jie

Shanghai University of Traditional Chinese Medicine

yejie1977@126.com+86 13300180301

Outcome results

None listed

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