Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07536516

Measurement of Ocular Blood Flow and Retinal Oxygen Extraction in Diabetic Patients

Led by Medical University of Vienna · Updated on 2026-04-17

20

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The prevalence of diabetes is increasing, with type 2 diabetes mellitus comprising over 90% of cases. Diabetes mellitus complications, including diabetic retinopathy (DR), impose significant health burdens. GLP-1 receptor agonists (GLP-1RAs) and dual GIP/GLP-1 receptor agonists show promise in improving cardiovascular and kidney outcomes, but their effects on retinal microvasculature and neuroprotection remain unclear. This study investigates the impact of GLP-1RAs (semaglutide, liraglutide) and GIP/GLP-1-dual agonists (tirzepatide) on ocular blood flow and retinal function in DM patients.

CONDITIONS

Official Title

Measurement of Ocular Blood Flow and Retinal Oxygen Extraction in Diabetic Patients

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
  • Previously diagnosed diabetes mellitus
  • Normal eye exam except for diabetic retinopathy, unless abnormalities are clinically irrelevant
  • Planned start of therapy with GLP-1 receptor agonists (semaglutide, liraglutide) or GIP/GLP-1 receptor agonist (tirzepatide) by a diabetes specialist
Not Eligible

You will not qualify if you...

  • Participation in another clinical trial within 3 weeks before screening
  • Symptoms of a relevant illness within 3 weeks before the first study day
  • Severe medical conditions other than diabetes as judged by the investigator
  • Alcohol abuse
  • Blood donation in the previous 3 weeks
  • Any eye abnormalities preventing reliable measurements in the study eye
  • Previous laser photocoagulation treatment in the study eye
  • Best corrected visual acuity less than 0.4 Snellen
  • Women of childbearing potential not using effective contraception
  • Pregnancy, planned pregnancy, or breastfeeding

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

Medical University Vienna

Vienna, State of Vienna, Austria, 1090

Actively Recruiting

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Research Team

D

Doreen Schmidl, Prof. Priv. Doz. MD.; PhD

CONTACT

D

Doreen Schmidl, Prof. Priv. Doz. MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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