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Recruiting Observational

A Predictive Score for the Ischemic Etiology of a Transient Diplopia (VASCO-DIP)

NCT02576925 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2015-09-24
Last updated
2026-09-09

Condition(s) studied

Diplopia

Investigational drug(s) / intervention(s)

Clinical, ophthalmological and neurological evaluation

Clinical, ophthalmological and neurological evaluation: Clinical : questionnaire about the symptoms and about the vascular risk factors Imagery :Cerebral MRI, MRI angiography of the supra-aortic trunks, ECG, Holter, transthoracic echocardiography, Biology : blood count, erythrocytes sedimentation rate, C reactive protein Ophthalomogy : visual field, optical coherence tomography, retinography

Study summary

The transient diplopias (TD) is defined by a short diplopia. Their etiology may be ophthalmological, neurological non-ischemic or of ischemic origin.

The difficulty is to recognize an ischemic mechanism which imposes emergency cares.

A clinical score could help the clinician to recognize the etiology of the TD .

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Transient diplopia (i.e. less than 24 hours) during the last 8 days Exclusion Criteria: \-

Primary outcome measure(s)

  • Etiology, ischemic or not, of the initial transient diplopia — 3 months
    Questionnaire about the symptoms and about the vascular risk factors, cerebral MRI, MRI angiography of the supra-aortic trunks, ECG, Holter, transthoracic echocardiography, blood count, erythrocytes sedimentation rate, C reactive protein, visual field, optical coherence tomography, retinography and a new evaluation after 3 months.

Trial sites (2)

FacilityCityRegionStatus
Hôpital Bichat Paris France Recruiting
Fondation Ophtalmologique Adolphe de Rothschild Paris Île-de-France Region Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02576925 on ClinicalTrials.gov ↗ ← All trials in France