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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02228070
Other study ID # KEK-ZH-Nr. 2014-0481
Secondary ID
Status Completed
Phase N/A
First received August 25, 2014
Last updated October 24, 2017
Start date July 2015
Est. completion date July 2016

Study information

Verified date October 2017
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Measuring ocular motility and alignment is important for diagnosing different causes of strabismus, following patients recovering from cranial nerve palsies, preparing patients for strabismus surgery and follow-up post surgery. The current clinical gold standards for measuring ocular alignment are the Hess screen and the Harms tangent screen. These tests are accurate, but require patient cooperation, and are not objective because the patient has to indicate the position of the light he sees on the screen. Our objective is to develop an accurate and easy to use goggles system to measure ocular alignment and motility using 3D video oculography.


Recruitment information / eligibility

Status Completed
Enrollment 58
Est. completion date July 2016
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 11 Years and older
Eligibility Inclusion Criteria:

- Patients 11 years or older

- congenital strabismus

- acquired strabismus

- paretic strabismus (oculomotor, abducens and trochlear nerves)

- before and after strabismus surgery

- normal controls

Exclusion Criteria:

- Patients unable to sign informed consent

- Patients with significantly impaired vision

- Patients unable to cooperate with standard strabismus workup (including Hess and Harms tests)

- For sub-study: intolerance to scleral search coils

Study Design


Related Conditions & MeSH terms


Intervention

Device:
strabismus video goggles


Locations

Country Name City State
Switzerland Ophthalmology Department, University Hospital Zurich Zurich

Sponsors (3)

Lead Sponsor Collaborator
University of Zurich Albert Bruppacher-Stiftung, Stiftung OPOS zugunsten von Wahrnehmungsbehinderten

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Other Follow-up squint angle measures post-OP and after recovery from cranial nerve palsy with 3D video goggles and Hess/Harms screen Change in squint angle with 3D video goggles and Hess/Harms screen. initial visit, 3 months after surgery, recovery from cranial nerve palsy after 3 months
Primary Validation of video goggles against Hess/Harms screen Measurement of squint angle with 3D video goggles vs. Hess/Harms screen. initial visit
Secondary Accuracy of video goggles in comparison to scleral search coils Measurement of squint angle with 3D video goggles vs. scleral search coils. initial visit
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