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NCT07567833RecruitingPhase 4

Longitudinal Study of Retinal Function in Eyes Treated for Diabetic Macular Edema With Anti-VEGF Agents

Source: ClinicalTrials.gov · Last updated 23 Oct 2026

Brief summary (registry, in English)

A considerable hurdle to the development of novel, more effective therapies for diabetic retinal disease is the limited number of primary endpoints available for use in regulatory trials. Current endpoints necessitate long trial durations and a greater number of participants to show efficacy. Thus, a better understanding of the structural and functional changes in the retina occurring in people with diabetes is essential for developing primary endpoints and validating surrogate and clinical endpoints.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
First submitted
9 Feb 2026
Start date
31 Jul 2026
Primary completion date
31 Dec 2027
Lead sponsor
Jaeb Center for Health Research
NCT number
NCT07567833

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 100
  • From 31 Jul 2026 to the primary completion date, 31 Dec 2027
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous treatment of any kind for diabetic retinopathy or DME
  • Intraocular surgery (including cataract surgery) within 4 months prior to enrollment or anticipated within the next 6 months

Other illness

  • Ocular or systemic condition, aside from diabetes mellitus (DM), that is likely to affect the assessment of DRSS, DME, or the functioning of the neural retina.
  • Any condition that may preclude adequate imaging of the macula (e.g. dense cataract or other media opacity, ptosis)
  • History of rhegmatogenous retinal detachment or macular hole
  • History of vitrectomy

Who the study is looking for

  • Age ≥18 years
  • Diagnosed with Type 1 or Type 2 diabetes
  • Best corrected visual acuity 20/320 or better (Snellen) (≥24 ETDRS letters)
  • At least 1 eye with CI-DME requiring treatment
  • Able and willing to provide informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Southeast Retina Center, P.C.
Coordinator of this site? Confirm its status
AugustaUnited StatesRecruiting
Retina Consultants of Texas
Coordinator of this site? Confirm its status
BeaumontUnited StatesRecruiting
Boston Medical Center Corporation
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting
Henry Ford Health System
Coordinator of this site? Confirm its status
DetroitUnited StatesRecruiting
Retina Consultants of Southern California
Coordinator of this site? Confirm its status
Huntington BeachUnited StatesRecruiting
Retina-Vitreous Consultants, Inc.
Coordinator of this site? Confirm its status
MonroevilleUnited StatesRecruiting
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting
Pittsburgh Clinical Trial Consortium
Coordinator of this site? Confirm its status
SewickleyUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.