Optical Coherence Tomography And NEphropathy: The OCTANE Study

Sponsor
University of Edinburgh (Other)
Overall Status
Recruiting
CT.gov ID
NCT02132741
Collaborator
(none)
150
1
100
1.5

Study Details

Study Description

Brief Summary

Patients with high blood pressure (hypertension) and chronic kidney disease are at an increased risk of developing heart disease and strokes. Part of this risk is due to changes in the structure and function of the blood vessels throughout the body. It is thought that reducing high blood pressure and treating chronic kidney disease improves the structure and function of blood vessels but information on this is limited. Optical coherence tomography (OCT) is a method of looking at the blood vessels at the back of the eye. It is a simple, quick and non-invasive test that you may have previously had during a visit to the optician. The purpose of the study is to ascertain whether OCT is able to detect changes in the eye's blood vessels in patients with hypertension and chronic kidney disease compared to healthy individuals and also to see if any differences seen improve with treatment.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This project is an exploratory study, using enhanced depth imaging with the new SPECTRALIS OCT, designed to examine choroidal and microvascular retinal structure in patients with hypertension, chronic kidney disease (CKD), and in age and sex matched healthy controls. The study is non-invasive and takes only a few seconds to acquire these complex images. The Centre, where the images will be captured and where image analysis systems are located, is on the Royal Infirmary of Edinburgh (RIE) site close to the RIE outpatient clinics, making recruitment easy.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    150 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Assessment of Retinal Vasculature Using Optical Coherence Tomography in Health, Hypertension & Chronic Kidney Disease.
    Study Start Date :
    May 1, 2014
    Anticipated Primary Completion Date :
    May 1, 2022
    Anticipated Study Completion Date :
    Sep 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Treated hypertension

    Patients on treatment for hypertension

    CKD-ESRD

    Pre- & post haemodialysis

    Healthy individuals

    Healthy volunteers

    CKD

    Pre-dialysis CKD & those with a functional renal transplant

    Hypertension

    Untreated

    Outcome Measures

    Primary Outcome Measures

    1. Choroidal & retinal morphology [2 weeks]

      A composite measures outcome including: Sub-foveal choroidal thickness Choroidal volume Retinal vasculature morphology and optimality measurements (arteriolar thickness, branching coefficient and branching angle; fractal dimension, and venular tortuosity.)

    Secondary Outcome Measures

    1. Neuro-retinal metrics [2 weeks]

      A composite measures outcome of neuro-retinal metrics (retinal thickness, retinal nerve fibre layer thickness)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Male or female

    • Age 18-80

    • Body mass index ≤35

    • For those with hypertension: BP ≥140/90 or on treatment for hypertension

    • For those with CKD: CKD as defined by the Kidney Diseases Quality Initiative guidelines

    Exclusion Criteria:
    • Subject is below the age of legal consent, or is mentally or legally incapacitated

    • The subject has donated blood (450 ml) within the last 4 weeks

    • Past or present drug or alcohol abuse including intravenous drug abuse at any time

    • Participation in another clinical trial within 1 month

    • Considered to be at high risk of HIV or hepatitis B

    • Patients with known eye disease, or previous eye surgery, or refractive error greater than +/- 6 dioptres.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Edinburgh Edinburgh Midlothian United Kingdom EH164TJ

    Sponsors and Collaborators

    • University of Edinburgh

    Investigators

    • Principal Investigator: Neeraj Dhaun, MD PhD, University of Edinburgh

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Edinburgh
    ClinicalTrials.gov Identifier:
    NCT02132741
    Other Study ID Numbers:
    • 14/SS/0069
    First Posted:
    May 7, 2014
    Last Update Posted:
    Apr 14, 2021
    Last Verified:
    Apr 1, 2021
    Keywords provided by University of Edinburgh
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 14, 2021