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Clinical trialNCT03085784UnknownPhase 2Interventional

Intravitreal Aflibercept Injection for Radiation Retinopathy Trial

SponsorAmy C Schefler, MDEnrollment40Radiation Retinopathy
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The ARRT trial will assess the safety and efficacy of 2mg aflibercept for the treatment of radiation retinopathy, including maculopathy and optic neuropathy over 52 weeks.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

3 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Retina Consultants of Houston/texas Medical Center

    Houston, Texas, United States

  • Retina Consultants of Houston

    Katy, Texas, United States

  • Retina Consultants of Houston/the Woodlands

    The Woodlands, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
5 Jul 2017
Primary completion
31 Oct 2021
Completion
31 Oct 2021
Last update posted
8 Dec 2020
Registered enrollment
40
Registry id
NCT03085784

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.