Clinical Trial Details
— Status: Recruiting
Administrative data
| NCT number |
NCT03866005 |
| Other study ID # |
PROACTIVE-DME |
| Secondary ID |
|
| Status |
Recruiting |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
November 1, 2019 |
| Est. completion date |
November 1, 2021 |
Study information
| Verified date |
June 2020 |
| Source |
ZeaVision, LLC |
| Contact |
Jay M Haynie, OD |
| Phone |
(253) 572-1444 |
| Email |
drjay[@]soundretina.com |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
This study will evaluate the effects of add-on carotenoid plus anti-oxidant nutritional
supplementation to standard anti-vascular endothelial growth factor therapy for subjects with
center-involved diabetic macular edema
Description:
Diabetic retinopathy (DR) remains the leading cause of blindness in Americans of working age,
and the majority of people with diabetes are expected to develop retinopathy, with as many as
10% developing sight-threatening retinopathy (proliferative retinopathy and/or
center-involved macular edema) during their lifetime. Established risk factors for DR and
diabetic macular edema (DME) include duration of disease, metabolic control (particularly
severity and duration of hyperglycemia and hypertension), early age of diabetes diagnosis,
male gender, Black and Hispanic race/ethnicity, and albuminuria (kidney disease). , In
particular, DME accounts for the majority of vision loss due to diabetes, with significant
impacts on activities of daily living and quality of life. Approximately 30% of patients with
diabetes develop DME within twenty years of diagnosis.
Available treatments for DME include laser photocoagulation, intravitreal steroids via
injection or sustained release implant and, most importantly, intravitreal injection of
inhibitors of vascular endothelial growth factor (anti-VEGF). In a number of clinical trials,
serial injections of anti-VEGF agents have demonstrated superiority for both reducing
intra-retinal edema and improving/stabilizing visual acuity in patients with DME, and their
use has become the recognized standard of care, particularly when DME is at or very near the
foveal center (center-involved diabetic macular edema, CI-DME). However, anti-VEGF drugs for
DME typically require multiple injections, are expensive, carry small but measurable risk of
ocular and potentially systemic complications, and are not universally or adequately
effective.
A number of biochemical processes have been elucidated as contributing factors in DME,
including disruption of the cellular electron transport chain leading to excess production of
mitochondrial reactive oxygen and nitrogen species (ROS and RNS) that drives accumulation of
injurious glucose metabolites, with concomitant elevation of inflammatory cytokines,
leukostasis, apoptosis (programmed cell death), retinal capillary leakage and release of
vasoproliferative factors. More recent evidence has suggested that nutritional supplements
may interfere with the pathogenesis of structural and functional abnormalities associated
with diabetes and diabetic retinopathy. Specifically, use of a novel, multi-component, orally
administered nutritional supplement was shown to improve visual function (contrast
sensitivity, color perception, visual field) and serum markers of inflammation (hsCRP) in
patients with non-proliferative diabetic retinopathy without affecting blood glucose control
in an IRB-approved (Western IRB number 1129944 Olympia, WA) randomized, placebo-controlled
clinical trial (The Diabetes Visual Function Supplement Study [DiVFuSS]
Hypothesis
Our aim is to test the hypothesis that adjunctive supplementation with the DiVFuSS formula,
in addition to conventional anti-VEGF therapy with add-on laser photocoagulation and/or
intravitreal steroid as necessary, will result in reduced macular edema, fewer required
anti-VEGF injections and better visual acuity in treatment-naïve CI-DME subjects receiving
therapy over two years in a retinal specialty clinic. A secondary outcome to be assessed is
the percentage of patients requiring add-on laser or steroid treatment over the two years in
each of the study groups.
Overview of Study Design
This will be an investigator initiated, single-clinic/two location, double-blinded
prospective study of 150 adult subjects with newly diagnosed CI-DME receiving anti-VEGF
injections, with add-on laser and/or steroid as required on follow-up examination (Standard
Treatment) versus standard treatment plus adjunctive DiVFuSS supplementation in one of two
doses (2 softgels per day - Supplement Treatment Group 1; and 4 softgels per day - Supplement
Treatment Group 2). Subjects will be identified and enrolled with informed consent from two
retinal specialty practice sites in Washington State (Sound Retina; Tacoma, WA and Olympia,
WA). Subjects will be randomized to Standard Treatment; Supplement Treatment Group 1, or
Supplement Treatment Group 2.
Study Allocation: 150 treatment-naïve subjects with CI-DME Requiring anti-VEGF therapy
Standard Treatment Group (50 participants) with treatment-naive center-involved diabetic
macular edema will receive anti-VEGF therapy per specialists' usual protocol, with add-on
laser or steroid if necessary (at specialist's discretion); Supplement Treatment Group 1 (50
participants) with treatment-naive center-involved diabetic macular edema will receive
Standard Treatment plus two DiVFuSS softgels/day; Supplement Treatment Group 2 (50
participants) with treatment-naive center-involved diabetic macular edema will receive
Standard Treatment plus four DiVFuSS softgels/day.
After enrollment by the study Primary Investigator, a single retinal specialist from each
site, masked to subjects' supplement status, will deliver all treatments per his/her usual
protocol for treatment of CI-DME based on individual examination findings. Supplements will
be provided by ZeaVision, LLC of Chesterfield, MO. Subjects will receive detailed, dilated
eye examinations with additional customary tests (measurement of visual acuity, spectral
domain optical coherence tomography, high-resolution retinal photography) performed and
recorded by the masked Primary Investigator at baseline, 3 months, 6 months,12 months, 18
months and 24 months. Follow-up phone calls will be performed monthly between visits to help
assure compliance for the Test Supplement Treatment Groups (1 and 2). Wide-field fluorescein
angiography (FA) will be performed at baseline, 12 months and 24 months per usual care and
results recorded by the Primary Investigator.
Test Supplements
The adjunctive nutritional supplement will be the multi-component formula used in the
Diabetes Visual Function Supplement Study (Western IRB number 1129944 Olympia, WA),
containing the macular carotenoids lutein and zeaxanthin, as well as antioxidants (vitamins
B1, B12, C, D, E, lipoic acid, coenzyme Q10, resveratrol), omega3 fatty acids (EPA/DHA) and
botanical extracts (Pycnogenol™ [patented extract of French maritime pine bark, Pinus
pinaster], grape seed and green tea extracts, curcumin).
