Pupillometry in Horner's Syndrome

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

135 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-15

Study Completion Date

2022-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Insights From the Retina on Cerebral Microvascular Dysfunction in Haemorrhagic Stroke

NCT04363619

Intracerebral Hemorrhage

COMPLETED NA

Pupillometric Evaluation in Patients Declared Brain Dead - a Prospective Quality Control Study

NCT06279975

Brain Death Adults

RECRUITING

Investigation of Vascular Pathology in Eye Diseases Using Using Optical Coherence Tomography Angiography (OCT-A)

NCT02811536

Retinal Disease

COMPLETED

Monochromatic Digital-Pupillometry With Two Automated Devices in Comparison to Manual Measurements on Digital Photographs

NCT02978092

Pupil Examination

COMPLETED

Central Serous Chorioretinopathy: Etiology, Course and Prognosis

NCT01378130

Central Serous Chorioretinopathy

COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Horner's Syndrome Stroke Dissection Carotid Artery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Pupillometry in stroke patients

All eligible patients will undergo pupillometry test for the finding of Horner's syndrome

Group Type EXPERIMENTAL

Automated pupillometry

Intervention Type DEVICE

Automated pupillometry will be performed in patients with acute stroke with the intention of diagnosing Horner's syndrome

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Automated pupillometry

Automated pupillometry will be performed in patients with acute stroke with the intention of diagnosing Horner's syndrome

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adults 60 years of age or younger
* Acute stroke (less than 72 hours from admission)
* Informed Consent as documented by signature (Appendix Informed Consent Form)
* Ability to understand the study information and consent form

Exclusion Criteria

* known history of HS
* Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.
* Medications affecting pupillary response
* History of ocular surgery affecting the pupil

Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No