Evaluation of Tests Performance on a New Digital Orthoptic Platform

Evaluation de la Performance d'Une Nouvelle Plateforme de Tests de dépistage Orthoptique numériques

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02651389

Acronym

ESPPADON

Enrollment

Registered

2016-01-11

Start date

2016-02-18

Completion date

2016-09-29

Last updated

2017-04-14

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

Conditions

Binocular Vision Disorder, Visual Impairment

Keywords

Digital Orthoptic Platform, Vision test

Brief summary

This clinical trials aims to evaluate Tests Performance on a New Digital Orthoptic Platform.

Detailed description

The demography of ophthalmologists is becoming weaker, many tasks are now performed by orthoptists. To optimize the achievement of orthoptic exams and thus make reliable screening in a shorter time, digital tools are developed. They attempt to renew the orthoptic screening equipment that is still made up of numerous tests, often with old designs that must be handled and adapted to each patient which constitutes a significant loss of time. It therefore appeared necessary for us to develop a platform of digital tools that integrates major tests used for diagnostic purposes, especially a visual acuity test, a stereoscopic vision test, a fusion test and a digital synoptophore enabling a detailed analysis of disorders of binocular vision. The purpose of the study is to evaluate this new tool, avoiding the mobilization of patients , and quantify whether this platform is precise, reliable, fast, comfortable and allow the realization of a safe examination for the patient and for orthoptics.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

7 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Patients with less than or equal to 16 ocular deviation prism diopters, without or with slight amblyopia (maximum difference of 2 logarithmic visual acuity lines) and performing an orthoptic exam at ophthalmology department of Brest University Hospital.

Exclusion criteria

* monophthalmic * Medium and deep amblyopic patients * Patients with not normal ocular motility * Patient who underwent surgery at the head and neck during the previous three months * Children under 7 years old.

Design outcomes

Primary

Measure	Time frame
Correlation of Ocular Convergence as Measured by the Two Machines	through study completion, an average of 1 hour

Countries

France

Outcome results