Isolated Deficits of the Lateral Semicircular Canal
CSL
Evolutionary Profile of Isolated Lateral Semicircular Canal Deficits on the Video Head Impulsed Test (VHIT)
1 other identifier
observational
12
1 country
1
Brief Summary
There are only a few cases of isolated lateral canal deficit described in the literature. This study would focus on this group of patients in order to establish an evolving profile, a recovery behavior that we could compare to that in the literature. In addition, the evolving profile as well as the other clinical criteria identified would allow investigators to make hypotheses as to the pathology responsible for a given evolutionary profile. The population studied is represented by adult patients admitted by the emergency consultation service of otolaryngology of the University Hospitals of Strasbourg for an acute unilateral vestibular deficit whose examination at the VHOT shows a reduced and isolated gain of a lateral semicircular canal.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Sep 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2021
CompletedFirst Submitted
Initial submission to the registry
November 24, 2021
CompletedFirst Posted
Study publicly available on registry
December 8, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2022
CompletedDecember 8, 2021
November 1, 2021
1.2 years
November 24, 2021
November 24, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Establish the evolutionary profiles of patients with isolated lateral canal involvement
1 month
Eligibility Criteria
Patient treated in the ENT department for dizziness between June 2020 and July 2021.
You may qualify if:
- Major patient
- Man or woman
- Patient who has given their consent to the use of their data.
- Patient treated in the ENT department for dizziness between June 2020 and July 2021.
- Patient who expressed his opposition to participating in the study
- Inability to provide the subject with enlightened information (difficulties in understanding the subject, cognitive disorders)
- Subject under safeguard of justice
- Subject under guardianship or guardianship
- Neurological signs on clinical examination
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Oto-rhino-laryngologie et Chirurgie cervico-faciale - Hôpitaux Universitaires de Strasbourg
Strasbourg, 67091, France
Study Officials
- PRINCIPAL INVESTIGATOR
Anne CHARPIOT, MD, PhD
Oto-rhino-laryngologie et Chirurgie cervico-faciale - Hôpitaux Universitaires de Strasbourg
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 24, 2021
First Posted
December 8, 2021
Study Start
September 1, 2021
Primary Completion
November 1, 2022
Study Completion
November 30, 2022
Last Updated
December 8, 2021
Record last verified: 2021-11