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Diabetic Macular EdemaOCT and DMENCT01876914

Pilot Study of OCT Versus Fluorescein Angiography in DME

An observational study of Diabetic Macular Edema, run by Oregon Health and Science University at 1 site in United States.

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

Diabetic Macular Edema (DME), which can happen as a complication of diabetes, occurs when fluid and proteins collect in the macula (the yellow central area of the retina). The fluid can cause swelling which in turn can lead to worsening central vision. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Diabetic Macular Edema
How many people
20 participants
Where
1 siteUnited States
Study dates
Jun 2013to 23 Dec 2017
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Individuals 18 years of age and older presenting to the Retina Service within the Department of Ophthalmology at the Casey Eye Institute of Oregon Health \& Science University with signs and symptoms of DME will be evaluated for enrollment into this study. This pilot study has a planned enrollment target sample size of 28 subjects with DME. However, up to 35 subjects will be recruited as it is possible that after subjects sign the consent form they may not meet all eligibility criteria.

Who may be able to join

  • Diagnosis of diabetes mellitus (type 1 or type 2).

Who cannot join

  • Inability to give informed consent.
  • Inability to complete study tests within a 30 day period.
  • Inability to maintain stable fixation for OCT imaging.
  • Significant renal disease, defined as a history of chronic renal failure requiring dialysis or kidney transplant.
  • A prior history of reaction to fluorescein or other dyes.
  • A condition that, in the opinion of the investigator, would preclude participation in the study (e.g., unstable medical status including blood pressure, cardiovascular disease, and glycemic control).
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  • Blood pressure > 180/110 (systolic above 180 OR diastolic above 110). If blood pressure is brought below 180/110 by anti-hypertensive treatment, subject can become eligible.
  • Systemic anti-VEGF or pro-VEGF treatment within 4 months prior to treatment.
  • Women of child-bearing potential: pregnant or lactating or intending to become pregnant within the next 12 months due to unknown safety of fluorescein angiography.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Oregon Health & Science University

    Portland, Oregon, 97239

Other trials in United States

About this study

Official title: Pilot Study of OCT Versus Fluorescein Angiography in Diabetic Macular Edema in Eyes With Good and Poor Macular Capillary Perfusion

Diabetic Macular Edema (DME), which can happen as a complication of diabetes, occurs when fluid and proteins collect in the macula (the yellow central area of the retina). The fluid can cause swelling which in turn can lead to worsening central vision. The purpose of this study is to see if the study device (Swept Source Optical Coherence Tomography or SS-OCT) is able to diagnose DME as well as an already approved imaging procedure called fluorescein angiography (FA). FA is standard of care and would be conducted regardless of study participation. The dye used in FA, which can cause allergic reactions in some patients and is not used in pregnant women, is not needed with the study device. Another purpose of the study is to avoid the risk of administering the FA dye if possible.

Read the detailed description

Diabetic macular edema (DME) is one of the most common causes of visual loss in patients with diabetes and a leading cause of blindness in the working age population.

In DME, excess fluid from blood vessels in the retina leaks into the macula, causing swelling. Because the macula is responsible for sharp central vision, the swelling causes blurred or distorted of central vision, loss of contrast sensitivity, and can include changes in color perception. A patient with macular edema may or may not also have ischemia, an abnormal reduction in blood flow to the retina due to blockage of the retinal blood vessels. In macular ischemia, inadequate blood supply to the central retina results in a loss of retinal cell function and irreversible central vision loss. DME is most often treated with a focal laser application or an injection of an anti-vascular endothelial growth factor (anti-VEGF) drug into the eye to stop leaky vessels.

DME is currently diagnosed by slit-lamp biomicroscopy and optical coherence tomography (OCT). Conventionally, OCT is used to assess edema (retinal thickening and fluid pockets). The initial assessment and treatment planning also requires an assessment of macular perfusion, which is currently done by fluorescein angiography (FA). FA is used to identify microaneurysms and areas of capillary dropout (ischemia), which guides focal laser treatment and helps predict treatment response. Eyes with greater ischemia respond more poorly to treatment. FA requires the injection of sodium fluorescein into the systemic circulation. However, 1 in 3 people have adverse reactions to sodium fluorescein, which can include nausea, vomiting, hives, and acute hypotension. Severe reactions such as anaphylaxis, causing cardiac arrest and sudden death due to anaphylactic shock, have also been reported. Finally, because the risks of sodium fluorescein to a developing fetus are unknown, its use in pregnant women is contraindicated. Replacing FA with a less invasive and better tolerated method would reduce the risk in the patient population. One option is OCT angiography.

Optical coherence tomography is an imaging technology that can perform non-contact cross-sectional imaging of tissue structure in real time.It is analogous to ultrasound B-mode imaging, except that OCT measures the intensity of reflected light rather than acoustical waves. OCT has a number of features that make it attractive as a diagnostic imaging modality: 1.) It has micron-level resolution, which is not possible with any other non-contact technique; 2.) No potentially allergenic dyes or contrast agents are required; 3.) OCT images are generated in electronic form, which facilitates the use of digital image processing techniques to extract quantitative parameters regarding the imaged tissue anatomy. For these reasons, structural OCT is already routinely used to assess areas of macular edema and response to treatment. Novel functional OCT including Doppler OCT and OCT angiography may allow an assessment of retinal blood flow and obviate the need for the more invasive FA test.

Thus, if the diagnostic data provided by functional OCT are at least equivalent or superior to those achieved by FA, patients and healthcare providers could realize a substantial benefit in utilizing this technology in the management of DME. To clarify, FA is standard of care and is not a procedure in this protocol, rather simply a comparison is being conducted between functional OCT and FA.

Keywords
Diabetes, Edema, DME, OCT
Medical subject headings
Diabetes Mellitus, Edema

What participants receive

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

Study groups in NCT01876914
Study groupRoleWhat they receive
DME patientsPatients suspected to have a problem with at least one eye called diabetic macular edema or DME

What is being measured

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

  1. Total retinal blood flow & visual acuity

    Total retinal blood flow, as measured by Doppler OCT, is correlated with visual acuity and the area of macular ischemia as evaluated by FA. This will be performed by the following analysis:

    1. Pearson's correlation test of total retinal blood flow with logMAR visual acuity;
    2. Pearson's correlation test of total retinal blood flow with the area of macular ischemia on FA.

    Measured: 1 year

Secondary outcomes (2)
  1. Macular ischemic areas and microaneurysms, as identified by FA vs. OCT

    Macular ischemic areas and microaneurysms, as identified by OCT angiography, corresponds to ischemia areas and microaneurysms identified by FA; This will be performed by the following analysis:

    1. Pearson's correlation test of macular ischemic area with the area of capillary drop-out on FA;
    2. Pearson's correlation test of the number of microaneurysms identified by OCT angiograms with that identified by FA.

    Measured: 1 year

  2. The degree of parafoveal ischemia as identified by OCT and visual acuity

    The degree of parafoveal ischemia as identified by OCT angiography correlates to visual acuity.

    1. Pearson's correlation test of parafoveal retinal flow index quantified by OCT angiography with logMAR visual acuity;

    Measured: 1 year

Timeline

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

  1. First posted13 Jun 2013 (estimated)
  2. Study startJun 2013
  3. Primary completion23 Dec 2017
  4. Study completion23 Dec 2017

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
Case only
Time perspective
Prospective
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01876914
Sponsor's protocol ID
OHSU IRB #9361
Other IDs
8UL1TR000128-07
Acronym
OCT and DME
Status last verified
Apr 2018
First submitted
6 Jun 2013
Last updated
6 Apr 2018
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Diabetic Macular Edema, run by Oregon Health and Science University at 1 site in United States.

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 1 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 6 Apr 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. 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?

Total retinal blood flow & visual acuity (time frame: 1 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 6 Apr 2018.

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