Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID02132741

Assessment of Retinal Blood Vessels Using Optical Coherence Tomography in Health, Hypertension, and Chronic Kidney Disease

Led by University of Edinburgh · Updated on 2026-05-13

150

Participants Needed

1

Research Sites

35 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether optical coherence tomography (OCT), a simple and non-invasive imaging method of the eye's blood vessels, can detect changes in patients with high blood pressure (hypertension) and chronic kidney disease (CKD) compared to healthy individuals. The study aims to understand if these changes in blood vessels improve with treatment. This exploratory study focuses on the structure and function of blood vessels, which are linked to increased risks of heart disease and strokes in these patients. The study involves examining the choroidal and microvascular retinal structures using enhanced depth imaging with the SPECTRALIS OCT device. Participants include patients with treated hypertension, those pre- and post-haemodialysis, healthy volunteers, patients with pre-dialysis CKD or a functional renal transplant, and untreated individuals. The imaging takes only a few seconds and is conducted at the Royal Infirmary of Edinburgh outpatient clinics. During the study, participants will undergo OCT imaging to assess choroidal and retinal morphology as the primary outcome within 2 weeks. Neuro-retinal metrics will also be measured as secondary outcomes. The study is observational, non-invasive, and designed to capture detailed images easily. Participants may include healthy volunteers and patients aged 18 to 80 years, with monitoring focusing on retinal vasculature and its relation to hypertension and CKD.

CONDITIONS

Brief Title

Optical Coherence Tomography And NEphropathy: The OCTANE Study

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female
  • Age 18 to 80 years
  • Body mass index of 35 or less
  • For hypertension patients: blood pressure of 140/90 or higher or currently treated for hypertension
  • For chronic kidney disease patients: diagnosed according to Kidney Diseases Quality Initiative guidelines
Not Eligible

You will not qualify if you...

  • Under legal age or mentally/legal incapacitation
  • Donated 450 ml of blood within the last 4 weeks
  • History of drug or alcohol abuse including intravenous drug use
  • Participated in another clinical trial within the last month
  • Considered high risk for HIV or hepatitis B
  • Known eye disease, previous eye surgery, or refractive error greater than +/- 6 dioptres

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - A few seconds per imaging session

Participants undergo non-invasive imaging to examine retinal and choroidal blood vessels using Optical Coherence Tomography.

1 visit (in-person)

Long-term Monitoring

Duration - 2 weeks

Participants are observed to assess retinal morphology and neuro-retinal metrics over a 2-week period.

No additional visits required

Trial Site Locations

Total: 1 location

1

University of Edinburgh

Edinburgh, Midlothian, United Kingdom, EH164TJ

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Research Team

N

Neeraj Dhaun, MD PhD

D

David Webb

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

5

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Published Research Related To This Trial