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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03377166
Other study ID # 0113-17-TLV
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2018
Est. completion date December 19, 2018

Study information

Verified date January 2019
Source Tel-Aviv Sourasky Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A comparison between two methods evaluating SVV: Bucket Test and A smartphone-based test.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date December 19, 2018
Est. primary completion date December 19, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Vestibular Disorder

Exclusion Criteria:

- Chronic ear disease, Neurological disorder, s/p Ear surgery

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Bucket test and Smartphone-based evaluation of SVV
Bucket test and Smartphone-based evaluation of SVV

Locations

Country Name City State
Israel The Tel Aviv Sourasky Medical Center Tel Aviv

Sponsors (1)

Lead Sponsor Collaborator
Tel-Aviv Sourasky Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Results of Bucket test Smartphone-based evaluation of SVV 5 minutes
Primary Results of Smartphone-based evaluation of SVV 5 minutes