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Study identifier: NCT06874283 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Ocular Complications From Cancer Therapy - Patient Registry and Biobank

Condition: Graft Versus Host Disease in Eye · Ocular Complications · Inflammatory Dry Eye Disease  ·  Sponsor: University of Maryland, Baltimore

PhaseN/A
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

The purpose of this study is to collect data on patients seen at University of Maryland after undergoing cancer therapy. Previous medications, ocular history, medical history, clinical evaluations, surgical procedures and outcomes will be gathered on the patients who consent to participate. Potential subjects will be enrolled from the clinical practice of the investigator at the time of their eye examination visit. A standard of care exam will be performed pertinent to the reason for the visit. In addition to the standard of care exam, certain biological specimens (ocular surface wash, mucocellular material, corneal filaments, impression cytology, and/or blood) will be collected, stored, and analyzed to obtain immunologic, cellular, or molecular mechanistic insights into disease pathogenesis.

This description comes directly from the study's public registry record.

Talk to the study team

Sarah Sunshine, MD  ·  667-214-1292  ·  ssunshine@som.umaryland.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Stoler Outpatient Cancer Center at the University of MarylandBaltimore, Maryland, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06874283