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Ocular Complications From Cancer Therapy - Patient Registry and Biobank

NCT06874283

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Graft Versus Host Disease in Eye
  • Ocular Complications
  • Inflammatory Dry Eye Disease

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 years and older
Sex
All
Healthy volunteers
Accepted
Sponsor
University of Maryland, Baltimore
Last updated on ClinicalTrials.gov
March 5, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Maryland · 1

  • Stoler Outpatient Cancer Center at the University of Maryland · Baltimore, MD

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.