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Yishenyangsui recipe for cervical myelopathy: A multicentre, prospective, randomized, placebo-controlled study

The research of traditional Chinese medicine comprehensive program in the prevention and treatment for cervical myelopathy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16009723
Enrollment
Unknown
Registered
2016-11-03
Start date
2016-11-05
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

cervical myelopathy

Interventions

Control group:Placebo (one bag at a time, twice a day, eight weeks) and mecobalamine pill (one pill at a time, three times a day, eight weeks)

Sponsors

Wangjing Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. all the subjects will be accordance with the diagnosis of cervical myelopathy; 2. aged from 40 to 70 old years; 3. sign the informed consent and refuse surgery.

Exclusion criteria

Exclusion criteria: 1. confirmed tumor in cervical spine, tuberculosis, or osteomyelitis; 2. spinal injury, fracture, or dislocation; 3. severe heart, pulmonary, brain, liver, kidney, or hematologic system disorders; 4. serious skin damage, infection or skin diseases; 5. have received cervical surgery treatment and cervical congenital malformation; 6. clear surgical indications: Frankel classification of spinal cord injury exceed D class, urinary and fecal incontinence, spinal cord compression ratio is below 0.4, no effective after at least three-month conservative treatment, and the symptoms become progressively aggravated.

Design outcomes

Primary

MeasureTime frame
Japanese Orthopaedic Association score;Neck Disability Index;

Countries

China

Contacts

Public ContactLiguo Zhu

Wangjing Hospital, China Academy of Chinese Medical Sciences

tcmspine@163.com+86 010-84739194

Outcome results

None listed

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