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Symptom Patterns Across Four Provocative Maneuvers for Laterality Assessment in Benign Paroxysmal Positional Vertigo: A Prospective Study of 569 Cases

Application of Visual Abnormality Markers for Rapid Localization of the Affected Canal and Side in Benign Paroxysmal Positional Vertigo

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600130084
Enrollment
Unknown
Registered
2026-08-14
Start date
2025-04-02
Completion date
Unknown
Last updated
2026-08-24

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

Conditions

Benign Paroxysmal Positional Vertigo

Interventions

Sponsors

The 988th Hospital of the Joint Logistics Support Force of the Chinese People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Participants were recruited from BPPV patients attending the vertigo clinic of a single tertiary hospital. Diagnosis followed the 2017 American Academy of Otolaryngology–Head and Neck Surgery (AAO-HNS) Clinical Practice Guideline update and the 2017 Chinese Medical Association guideline: (1) Age >= 18 years; (2) Presenting complaint of vertigo or dizziness; (3) Self-reported recurrent brief vertigo or dizziness provoked by head-position changes relative to gravity (e.g., getting up, lying down, turning in bed, looking up, bending forward).

Exclusion criteria

Exclusion criteria: (1) Conditions precluding safe positioning tests: cervical stenosis, severe cervical spondylosis, spinal deformity, morbid obesity (BMI >= 40 kg/m²), or known severe cerebrovascular disease; (2) Comorbidities potentially interfering with symptom reporting: vestibular migraine, active Ménière's disease, central positional vertigo, persistent postural-perceptual dizziness (PPPD), severe cognitive or language impairment, or severe psychiatric illness; (3) Recent intervention history: canalith repositioning within 1 week, vestibular suppressant medication within 48 hours, or vestibular rehabilitation within 1 week; (4) Pregnancy.

Design outcomes

Primary

MeasureTime frame
concordance rate between symptom asymmetry and the affected side;

Countries

China

Contacts

Public ContactZhang Peng

The 988th Hospital of the Joint Logistics Support Force of the Chinese People's Liberation Army

dr.peng2020@qq.com+86 371 8165 3164

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026