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Clinical study on the treatment of degenerative scoliosis by meridian acupoint spinal vibration therapy combined with'spinal balancing and guiding technique'

Clinical study on the treatment of degenerative scoliosis by meridian acupoint spinal vibration therapy combined with'spinal balancing and guiding technique'

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000271
Enrollment
Unknown
Registered
2024-08-20
Start date
2023-10-27
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

degenerative scoliosis

Interventions

control group:Spinal Balance Guiding Technique
experimental group:Meridian-based spinal vibration therapy combined with 'Spinal Balance Guiding Technique'

Sponsors

Longhua Hospital, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria: (Reference: Xu Shao-Ting Ge Bao-Feng Xu Yin-Tu-Kan eds. Practical Orthopaedics 3rd edition [M]. Beijing: People's Military Medical Press2005.03.) 1.1. It is found in middle-aged and elderly people over 40 years old; 1.2 Lumbar pain is characterised by postural lumbar pain which is aggravated by prolonged sitting walking and exertion. The pain usually occurs in the area where the deformity is most severe; 1.3 The symptoms of lower limbs are various pains and numbness and the femoral nerve pulling test or straight leg raising test may be positive; 1.4. Scoliosis with a coronal Cobb's angle >10° is seen on radiographs. 2. Coronal Cobb angle of 10°-30° on x-ray film; 3. Age: 40-80 years old; 4. No previous history of scoliosis scoliosis that occurs after adulthood; 5. Have not received any medication in the past 3 months; 6. Informed consent and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Those who have participated or are participating in other clinical studies in the last 3 months and those who have received or are receiving other treatments that affect the determination of efficacy in the last 3 months; 2. Patients with surgical indication (with obvious low back pain and radicular symptoms that cannot be relieved by treatment cobb angle greater than 30°-40° lateral slip greater than 6mm and progression of scoliosis angle greater than 10° ); 3. History of severe thoracolumbar spine trauma and thoracolumbar spine surgery fracture or placement of plate after fracture surgery and non-healing fracture; 4. Scoliosis secondary to organic spinal bone or soft tissue lesions such as tumours trauma tuberculosis Paget's disease and other causes; 5. History of opioid analgesics sedative-hypnotics and alcohol abuse; 6. Combined with high fever infectious diseases (such as arthritis discitis osteomyelitis septic arthritis) haemorrhagic disease severe cardiovascular and cerebrovascular dysfunction polyneuropathy skin ulcers or allergies open trauma during the period of anticoagulant medication installation of cardiac pacemaker cardiac bypass grafting intravascular stents mental disorders and other special physical conditions; 7. Congenital scoliosis or undetected adolescent idiopathic scoliosis; 8. Combined rheumatoid arthritis (ankylosing spondylitis rheumatoid arthritis etc.); 9. chondrodysplasia severe osteoporosis pathological inability of bones to bear the weight of the body cranial and facial sutures;

Design outcomes

Primary

MeasureTime frame
SF-36;

Secondary

MeasureTime frame
CFI;VAS;

Countries

China

Contacts

Public Contactqi-xin shen

Longhua Hospital, Shanghai University of Traditional Chinese Medicine

qixin_shen@126.com13761035717

Outcome results

None listed

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