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NCT02978079

Pupillometry in Horner's Syndrome

Status unknown NA Last updated 11 January 2021
What this trial tests

NA trial testing Automated pupillometry in Horner's Syndrome in 135 participants. Status unknown.

Timeline
15 February 2017
Primary endpoint
31 December 2021
31 December 2022

Quick facts

Lead sponsorUniversity of Zurich
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment135
Start date15 February 2017
Primary completion31 December 2021
Estimated completion31 December 2022
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

University of Zurich

Who can join

Adults 18 to 60, any sex, with Horner's Syndrome or Stroke. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Horner's syndrome (HS) is a result of interruption of the sympathetic innervation to the eye and ocular adnexa, which can occur due to carotid artery dissection (CAD), along which the sympathetic nerve fibers travel to reach the eye. Dissection of the carotid artery is one of the etiologies for ischemic stroke in young patients. In our current study, we will explore the diagnostic accuracy of automated binocular pupillometry in the diagnosis or HS, and its potential in identifying dissection of the carotid artery in patients of young age who suffer ischemic stroke.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other University of Zurich trials

Trials by the same sponsor.

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Data sources for this page

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