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Clinical study on the treatment of residual dizziness after manual reduction of benign paroxysmal positional vertigo with Wenpi Huayin formula

Clinical study on the treatment of residual dizziness after manual reduction of benign paroxysmal positional vertigo with Wenpi Huayin formula

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001136
Enrollment
Unknown
Registered
2025-06-07
Start date
2024-02-01
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Residual dizziness of benign paroxysmal positional vertigo

Interventions

Test group:traditional Chinese medicine
control group:Betahistine Mesylate

Sponsors

BeijingHuairouHospitalofTraditionalChineseMedicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Meets the diagnostic criteria for BPPV in Western medicine; Meets the diagnostic criteria for dizziness in traditional Chinese medicine; Meets the diagnostic criteria of traditional Chinese medicine syndrome. 2) Meets the diagnostic criteria for residual dizziness after manual reduction of benign paroxysmal positional vertigo; 3) Age between 18-80 years old male or female not limited; 4) Voluntarily participate in this experiment and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Secondary benign paroxysmal positional vertigo (s-BPPV) with a clear etiology. 2) Dizziness caused by Meniere's disease vestibular neuron inflammation cerebellar infarction brain tumors traumatic brain injury cerebral hemorrhage and certain autonomic nervous system diseases such as Parkinson's disease (PD) multiple system atrophy and other reasons; 3) Merge patients with other serious diseases such as lung heart liver kidney and blood disorders; 4) Patients with severe combined liver and kidney dysfunction (note: Liver dysfunction refers to ALT or AST values greater than twice the normal upper limit; Renal insufficiency refers to a blood creatinine level greater than twice the upper limit of normal; 5) Patients with severe cognitive impairment or serious mental illnesses; 6) Patients who are taking drugs that affect the autonomic nervous system such as anticholinergic drugs beta receptor antagonists and drugs that affect HCY UA NLR and PLR observation indicators; 7) Patients who are allergic to the ingredients in our formula; 8) Pregnant or lactating women; 9) Participants in clinical trials of other drugs. 10) Those who cannot and/or are unwilling to cooperate.

Design outcomes

Primary

MeasureTime frame
Duration of residual dizziness;

Secondary

MeasureTime frame
uric acid;platelet-lymphocyte ratio,PLR;dizziness handicap inventory;Dizziness Visual Analog Scale; Homocysteine;Score of Traditional Chinese Medicine Dizziness Grading Scale;neutrophil-lymphocyte ratio,NLR;

Countries

China

Contacts

Public ContactHao Shanshan

BeijingHuairouHospitalofTraditionalChineseMedicine

529752529@qq.com18801429367

Outcome results

None listed

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