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Clinical observation for dingxuan decoction in the treatment of vertebral artery type cervical spondylosis (turbidity of phlegm)

Clinical observation for dingxuan decoction in the treatment of vertebral artery type cervical spondylosis (turbidity of phlegm)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019662
Enrollment
Unknown
Registered
2018-11-21
Start date
2018-11-26
Completion date
Unknown
Last updated
2018-11-26

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

Conditions

Cervical Spondylotic Arteriopathy

Interventions

Group 1:Dingxuan granule (1 bag at a time, 2 times a day for 2 weeks)
Group 2:Betastine mesylate tablets (2 tablets at a time, 3 times a day for 2 weeks)

Sponsors

Wangjing Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1) meet the above diagnostic criteria; 2) aged 35 to 55 years; 3) disease duration: 5 years; 4) if you have received other conservative treatment, you will have a washout period of more than 5 days; 5) signing informed consent.

Exclusion criteria

Exclusion criteria: 1) other types of cervical spondylosis; 2) cervical vertebra has dislocation, fracture, tuberculosis, acute cervical intervertebral disc herniation, infection and tumor; 3) patients with vertigo caused by otogenic, cerebral, traumatic, ocular, neurogenic and intracranial tumors; 4) subclavian artery stealing blood syndrome; 5) patients with severe heart, liver, brain and kidney complications and other serious diseases; 6) pregnant and mentally ill; 7) patients allergic to traditional Chinese medicine or betastine mesylate tablets.

Design outcomes

Primary

MeasureTime frame
Cervical vertigo symptom and function scale;Quality of life scale sf-12;

Countries

China

Contacts

Public ContactZhang Wei

Beijing University of Chinese Medicine

sixdonkey@sina.com+86 13011802886

Outcome results

None listed

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