Actively Recruiting

Age: 18Years +
All Genders
NCT06398223

Ocular Perfusion in Patients With Unilateral Carotid Artery Stenosis

Led by Medical University of Vienna · Updated on 2024-05-03

45

Participants Needed

1

Research Sites

107 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the presented study is to evaluate ocular blood flow, respectively optic nerve head blood flow in patients with carotid artery stenosis before and after carotid endarterectomy or carotid artery stenting. Additionally, the investigators aim to compare optic nerve head blood flow in patients with CAS and healthy age- and sex-matched control subjects. Furthermore, the investigators intend to evaluate brain tissue oxygenation in patients with carotid artery stenosis before, during and after CEA and carotid artery stenting. Finally, the investigators will assess potential correlations between LSFG and NIRS results in patients with unilateral carotid artery stenosis.

CONDITIONS

Official Title

Ocular Perfusion in Patients With Unilateral Carotid Artery Stenosis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and women aged 18 years or older
  • Signed informed consent
  • Normal eye health unless any abnormality is deemed clinically irrelevant by the investigator
  • Diagnosis of unilateral carotid artery stenosis and planned carotid endarterectomy or carotid artery stenting
  • For healthy controls: normal medical history unless any abnormality is deemed clinically irrelevant
  • For healthy controls: non-smokers
Not Eligible

You will not qualify if you...

  • Blood donation within three weeks before the study
  • Symptoms of any clinically relevant illness within three weeks before the study
  • Eye inflammation or infection within the past three months
  • Personal or family history of epilepsy
  • Diagnosis of type 1 or type 2 diabetes mellitus
  • Pregnant or breastfeeding women
  • Women of childbearing potential who are not using effective contraception and are neither menopausal, hysterectomized, nor sterilized

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Clincal Pharmacology, Medical University of Vienna

Vienna, Austria, 1090

Actively Recruiting

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Research Team

G

Gerhard Garhöfer, Assoc. Prof. Priv. Doz. MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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