RECRUITING

Adaptive Optics Retinal Imaging

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Background: \- By the time diseases of the retina are detected, serious damage has often already been done. Researchers want to find better ways of viewing the retina. One way called adaptive optics may help detect problems earlier. Objectives: \- To study if adaptive optics can help find better ways to diagnose, treat, and manage retinal diseases. Eligibility: * People over age 12 with an eye disease. * Healthy volunteers over age 12. Design: * Participants will be screened with medical history and eye exams. These may include dilating pupils and taking pictures of the eyes. * Participants will have 1 or more study visits. They will have: * Medical and eye history. * Questions about their medications. * Eye exam including pupil dilation. * Adaptive optics imaging. After dilation, participants sit still while looking into an adaptive optics instrument. They look at specific places and images are taken of their retina. * They may also have: * More images. * Perimetry. Participants look into a lens and press a button when they see a light. * Color vision tests. * Electroretinogram. Participants will get numbing eye drops and special contact lenses. A small metal electrode will be put on their forehead. They will look at flashing lights and try not to blink.

Official Title

Adaptive Optics Retinal Imaging

Quick Facts

Study Start:2015-02-20
Study Completion:2028-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT02317328

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years to 120 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Are 12 years of age or older.
  2. * Have the ability to cooperate with an eye exam and adaptive optics imaging.
  3. * Have the ability to understand and sign an informed consent or have a parent/legal guardian to do so if they are minor children.
  4. * Have an eye disease or are a healthy volunteer with a normal eye exam (no visually-significant eye findings on examination).
  1. * Are under 18 years of age.
  2. * For participants who will undergo fluorescein imaging have a history of adverse reaction to fluorescein.
  3. * For participants who will undergo indocyanine green imaging have a history of adverse reaction to indocyanine green dye, know or suspected allergies to iodine or shellfish.

Contacts and Locations

Study Contact

Daniel W Claus, R.N.
CONTACT
(301) 451-1621
daniel.claus@nih.gov
Johnny C Tam, Ph.D.
CONTACT
(301) 435-7821
johnny.tam@nih.gov

Principal Investigator

Johnny C Tam, Ph.D.
PRINCIPAL_INVESTIGATOR
National Eye Institute (NEI)

Study Locations (Sites)

National Institutes of Health Clinical Center
Bethesda, Maryland, 20892
United States

Collaborators and Investigators

Sponsor: National Eye Institute (NEI)

  • Johnny C Tam, Ph.D., PRINCIPAL_INVESTIGATOR, National Eye Institute (NEI)

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2015-02-20
Study Completion Date2028-03-31

Study Record Updates

Study Start Date2015-02-20
Study Completion Date2028-03-31

Terms related to this study

Keywords Provided by Researchers

  • Eye Disease
  • Natural History

Additional Relevant MeSH Terms

  • Eye Diseases
  • Healthy Volunteers