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Clinical trial of Banxia Baizhu Tianma formula particles for the treatment of acute episodes of vertigo (the wind-phlegm syndrome) clinical efficacy and safety of multi-center, randomized, positive drug control clinical research program

Chinese medicine formula particles national standard upgrade and comparative study of curative effect of clinical decoction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014262
Enrollment
Unknown
Registered
2018-01-02
Start date
2018-01-02
Completion date
Unknown
Last updated
2018-01-08

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

Conditions

Acute Episodes of Vertigo(the wind-phlegm syndrome)

Interventions

treatment group:Banxia Baizhu Tianma formula particles (Shineway brand)
control group:Banxiabaizhu Tianma Decoction (traditional herbs decoction)

Sponsors

Shijiazhuang Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Meet Western diagnostic criteria of posterior circulation ischemia; (2) Meet the vertigo diagnostic criteria of Chinese medicine; (3) In line with the syndrome of the wind-phlegm syndrome of TCM syndrome in acute episodes of vertigo (can be combined with other syndromes), have not received any for the treatment of vertigo light, moderate patients (level of stun grading 0-III level); (4) 18 years old to 80 years old, male or female; (5) Patients or their families with informed consent, and signed Informed Consent Forms.

Exclusion criteria

Exclusion criteria: (1) Except posterior circulation ischemia other diseases such as: intracranial space-occupying lesions, brain trauma, brain inflammation, cervical spondylosis, ear diseases such as Meniere's disease, labyrinthitis, vestibular neuron inflammation, chain Mycotoxin and other diseases caused by vertigo; (2) Dizziness caused by transient ischemic attack (TIA); (3) Significant depression, severe neurological deficits can not complete the examination, such as coma, a variety of aphasia, audio-visual disorders; (4) Those who can not swallow oral drugs, or suffering from diseases that affect the absorption of oral drugs, such as active bowel disease, partial or complete intestinal obstruction; (5) Severe circulatory, respiratory, urinary, digestive, hematopoietic (eg unstable angina, uncontrollable asthma, active gastric bleeding, etc.) and cancer; (6) Severe bleeding tendency and liver and kidney dysfunction (aminotransferase more than 1.5 times the upper limit of normal, creatinine clearance = 133mmol/L); (7) Pregnancy, lactation or pregnancy may be pregnant and planning patients; (8) Participate in other clinical studies or participate in other clinical studies within 3 months prior to the date of informed consent; (9) Researchers think it inappropriate to participate in this study;

Design outcomes

Primary

MeasureTime frame
Improve TCM syndrome score before and after treatment;

Secondary

MeasureTime frame
The improvement of the comprehensive effect of vertigo before and after treatment (integral of vertigo symptom + main complication symptom score);The improvement of vertigo symptom scores before and after treatment;UCLA vertigo scale before and after treatment;Drugs to drug recurrence rate of 4 weeks;Drugs to drug recurrence rate of 12 weeks;

Countries

China

Contacts

Public ContactJianjing Yao

Shijiazhuang Hospital of Traditional Chinese Medicine

670344215@qq.com+86 15133196552

Outcome results

None listed

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