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A Study to Evaluate Optical Coherence Tomography (OCT) and OCT Angiography (OCTA) Imaging In Supine Patient

Overview

About this study

The purpose of this study is to determine if a relay lens and right angle mirror can be used in conjunction with an FDA-approved optical coherence tomography (OCT) unit to allow imaging in supine patients.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Medical indication for examination under anesthesia and OCT/OCTA imaging, including an ocular oncology or retinal disorder, such as retinoblastoma.
  • Control images will be obtained from patients with an indication for OCT/OCTA imaging who are able to cooperate for images in the office.

Exclusion Criteria: 

  • Patients who do not have a medical indication for OCT/OCTA imaging.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Lauren Dalvin, M.D.

Open for enrollment

Contact information:

Lauren Dalvin M.D.

(507)284-2233

Dalvin.Lauren@mayo.edu

More information

Publications

Publications are currently not available

More about research at Mayo Clinic

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CLS-20462231

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