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Comparison of treatment outcomes for PC-BPPV-cu type

Comparison of treatment outcomes for PC-BPPV-cu type

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011893
Enrollment
60
Registered
2026-04-22
Start date
2026-01-19
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

None listed

Interventions

Procedure/Surgery : This study is a randomized, parallel-group interventional study designed to compare the efficacy of a conventional treatment and a newly developed treatment in patients with poster

Sponsors

Inje University Ilsan Paik Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Adults aged 19 years or older who are able to understand and provide informed consent (2) Patients diagnosed with posterior canal cupulolithiasis (PC-BPPV-Cu) according to the diagnostic criteria proposed by the Bárány Society in 2015 The diagnosis must meet the criteria established by the Bárány Society in 2015, which are as follows: A. Recurrent attacks of positional vertigo or positional dizziness, provoked by lying down or turning over in the supine position. B. Positional nystagmus elicited after a brief or no latency by a “half Dix-Hallpike maneuver”, beating torsionally with the upper pole of the eye to the lower ear and vertically upward (to the forehead) and lasting > 1 min. C. Not attributable to another disorder.

Exclusion criteria

Exclusion criteria: (1) History of other otologic or medical conditions that may cause dizziness (e.g., anemia, orthostatic hypotension, Ménière’s disease, vestibular neuritis, etc.) (2) Cases in which a central cause of dizziness is suspected (3) Individuals who are unwilling to participate or do not provide informed consent (4) Individuals with psychiatric disorders (5) Any other cases deemed inappropriate for participation in the study at the discretion of the principal investigator

Design outcomes

Primary

MeasureTime frame
The number of repositioning maneuvers required until complete resolution of BPPV

Secondary

MeasureTime frame
Time to symptom improvement (days);Change in dizziness VAS score;Treatment-related adverse events

Countries

Korea, Republic of

Contacts

Public ContactJeon Mi Lee

Inje University Ilsan Paik Hospital

meowmiya@paik.ac.kr+82-31-910-7250

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: May 1, 2026