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NPDR - Non Proliferative Diabetic RetinopathyCHARTNCT04636307

Characterization of Retinal Disease Progression in Eyes With Non Proliferative Diabetic Retinopathy in Diabetes Type 2 Using Non-invasive Procedures (CHART)

An observational study of NPDR - Non Proliferative Diabetic Retinopathy and Diabetes Mellitus, Type 2, run by Association for Innovation and Biomedical Research on Light and Image at 5 sites in 3 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

To identify biomarkers, obtained using non-invasive procedures, that can predict disease progression and progression to sight-threatening stages of the disease and to characterize the retinal changes that occur in Non Proliferative Diabetic Retinopathy (NPDR). Read more about this study

Who is it for?
Ages 35 to 90 years
What is being tested?
Biomarkers
How many people
202 participants
Where
5 sitesin 3 countries
Study dates
22 Sep 2021to 22 May 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 35 to 90 years
  • All sexes
  • Adult, Older adult

Study population: Diabetes Type-2 and NPDR (levels 35, 43, 47 or 53)

Who may be able to join

  • Diabetes type 2 according to 1985 WHO criteria;
  • Age between 35 and 90 years;
  • NPDR levels 35, 43, 47 or 53 (based on the ETDRS criteria - 7 fields CFP) after confirmation by the Reading Centre;
  • Refraction with a spherical equivalent less than 5 Dp;
  • Informed consent.

Who cannot join

  • Repeated HbA1C > 10% in the first visit;
  • Cataract or other eye disease that may interfere with fundus examinations;
  • Age-related macular degeneration, glaucoma, vitreomacular disease, or other retinal vascular disease, or any ocular condition that, in the opinion of the investigator may affect retinopathy status or alter visual acuity during the study;
  • Any eye surgery within a period of 6-months;
  • Previous laser treatment or previous intravitreal injections;
  • Any patient comorbidity likely to affect the eye and not related with diabetes or cardiovascular disease;
Show all 9Show fewer
  • Presence of CIME (CRT ≥ 290 μm in women and ≥ 305 μm in men) with vision loss or needing immediate treatment, according to clinical practice;
  • Dilatation of the pupil < 5 mm;
  • Uncontrolled systemic hypertension (values outside normal range: systolic 70-210 mmHg and diastolic 50-120 mmHg).

Trial locations and contacts

5 sites in 3 countries.

5 sites in 3 countries

Italy3 sites
  • CS067- Department of Ophthalmology, University Vita Salute - Scientific Institute of San Raffael, Milan

    Milan

  • CS063 - Excellence Eye Research Centre, University G. d'Annunzio of Chieti-Pescara

    Pescara

  • CS020 - G. B. Bietti Eye Foundation - IRCCS

    Roma

Other trials in Italy

France1 site
  • CS042 - Department of Ophthalmology, University Hospital, CHU Dijon

    Dijon

Other trials in France

Portugal1 site
  • CS001 Centre for Clinical Trials - AIBILI

    Coimbra

Other trials in Portugal

About this study

Official title: Characterization of Retinal Disease Progression in Eyes With Non Proliferative Diabetic Retinopathy (NPDR) in Diabetes Type 2 Using Non-invasive Procedures (CHART)

To identify biomarkers, obtained using non-invasive procedures, that can predict disease progression and progression to sight-threatening stages of the disease and to characterize the retinal changes that occur in Non Proliferative Diabetic Retinopathy (NPDR).

Read the detailed description

The progression of diabetic retinopathy (DR) varies between different patients, even with similar metabolic control. It is becoming clear that a sizeable proportion of patients with mild non-proliferative diabetic retinopathy (NPDR) will take a long time to develop any sight-threatening complication. The inclusion of eyes/patients in a clinical trial that do not show any significant worsening during the period of the trial masks any beneficial effect of the drug being tested and consequently would increase trial sizes as the true therapeutic effect in high-risk patients would be partially obscured. It appears that the only option is to identify the eyes/patients that show progression of retinopathy during a pre-trial run-in period and only include such patients. Characterization of progressors in the early stages of DR and identification of biomarkers of disease progression are of major interest to facilitate drug development in this area of high unmet need.

Three different phenotypes of mild NPDR progression with different risks for development of Clinically Significant Macular Edema (CSME) were identified using cluster analysis based on the turnover rate of microaneurysms (MAT) and the central retinal thickness (CRT). Phenotype A, patients with low MAT and CRT < 260 micron in women and < 275 micron in men (on Cirrus Optical Coherence Tomography - OCT, corresponding to the mean CRT in healthy subjects plus 1 standard deviation, SD); Phenotype B, patients with low MAT and CRT ≥ 260 micron in women and ≥ 275 micron in men; and Phenotype C patients with high MAT. These phenotypes were recently confirmed in a larger population of NPDR patients. In this study, Phenotype B shows a risk for DR progression to Macular Edema (ME) of OR=13.30 and Phenotype C of OR=6.32. When CRT increase is present, then Phenotype C shows a higher risk for ME (OR=29.02). In these studies, the occurrence of proliferative diabetic retinopathy (PDR) as an outcome was rare and did not allow statistical analysis. More recently it was shown that phenotype C identifies eyes at higher risk for development of CSME and PDR, whereas phenotype A identifies eyes at very low risk for vision-threatening complications.

Patients with phenotypes B and C are, therefore, the NPDR patients with higher risk for ME development and are those patients who may benefit from early therapeutic or preventive treatment. Therefore, a proper characterization of this population is of major interest for the understanding of the disease, and to the design of new therapeutical approaches that can facilitate adequate and timely interventions.

To better characterize these patients, new non-invasive methods are now available that allow for a better insight of the retinal changes that occurs in these patients. The Optical Coherence Tomography Angiography (OCT-A) and OCT-Leakage (OCT-L) are two of these methods that can be used in longitudinal studies. These methods allow to quantify capillary closure and leakage, the main alterations occurring in DR (ischemia and leakage) and which are considered to predict sight-threatening complications, ME and PDR. In recent studies it was shown that the vessel density in the superficial and deep layers, obtained with OCT-A, and the Low Optical Reflectivity (LOR) ratio obtained with OCT-L are altered even in the earlier stages of DR. These two methods are therefore expected to better characterize leaky and ischemic patients' phenotypes (i.e., phenotypes B and C, respectively), being therefore a major step in early diagnosis and timely treatment of DR patients. Measurement of neurodegeneration (ND) represented by thinning of Ganglion Cell Layer (GCL) and Inner Plexiform Layer (IPL) will also be performed.

This study aims to better characterize the retinal changes that occur during a 2-years follow-up period in patients with diabetes Type 2 and with the initial stages of NPDR and at higher risk for sight-threatening complications, allowing better characterization of eyes at risk of progression (phenotypes B and C). The inclusion will be based on patients with established retinopathy ETDRS 35, 43, 47 and 53, distributed to the different clinical sites in the study, creating the opportunity to demonstrate the progression phenotypes.

Being tested
Biomarkers
Medical subject headings
Diabetes Mellitus, Type 2, Retinal Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BiomarkersOther

    To identify biomarkers obtained using non-invasive procedures that can predict disease progression and progression to sight-threatening stages of the disease and to characterize the retinal changes that occur in NPDR.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. DRSS severity progression

    DRSS severity progression of one, two or more ETDRS step changes

    Measured: 36 months

  2. Progression to vision-threatening complications

    CIME defined as eyes with a CRT ≥ 290 μm in women and ≥ 305 μm in men (Zeiss Cirrus SD-OCT); CSME identified on clinical evaluation as defined by ETDRS by retinal thickening within 500 μm of the center of the fovea or presence of hard exudates (with thickening of the adjacent retina) within 500 μm of the center of the fovea, or thickening of at least 1 disc area located less than 1 disc diameter from the center of the fovea. (Zeiss Cirrus SD-OCT); PDR identified by the presence of abnormal new vessels in the retina.

    Measured: 36 months

  3. Presence of ischemia

    dentified by decrease of 2 or more Standard deviations (in relation to healthy control population) on the values of vessel density, perfusion density or FAZ circularity.

    Measured: 36 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Nov 2020
  2. Study start22 Sep 2021
  3. Primary completion21 Mar 2023
  4. Study completion22 May 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
202 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04636307
Sponsor's protocol ID
ECR-RET-2020-15
Acronym
CHART
Status last verified
Dec 2025
First submitted
29 Oct 2020
Last updated
5 Dec 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Publications

  • Marques IP, Reste-Ferreira D, Santos T, Mendes L, Rocha AC, Bandello F, Parravano M, Mastropasqua L, Creuzot-Garcher C, Leal S, Baschiera F, Cunha-Vaz J. One-Year Progression of Capillary Nonperfusion in Nonproliferative Diabetic Retinopathy Using Noninvasive Imaging: The CHART Study. Transl Vis Sci Technol. 2026 Jan 5;15(1):26. doi: 10.1167/tvst.15.1.26.

    PubMed 41569021

Questions about this trial

What is this clinical trial studying?

An observational study of NPDR - Non Proliferative Diabetic Retinopathy and Diabetes Mellitus, Type 2, run by Association for Innovation and Biomedical Research on Light and Image at 5 sites in 3 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in Italy, France, Portugal. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

DRSS severity progression (time frame: 36 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04636307, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Dec 2025.

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