Can your phone spot eye cancer? app tested for retinoblastoma
NCT ID NCT03016156
First seen Jun 24, 2026 · Last updated Sep 16, 2026 · Updated 3 times
Summary
This study tested a smartphone app called CRADLE that uses a photo to detect leukocoria (a white glow in the pupil), which can be a sign of retinoblastoma, cataracts, or glaucoma. Researchers planned to compare the app's accuracy to a standard eye exam in children with these conditions. However, the study was terminated early after enrolling only 1 participant, so no reliable conclusions can be drawn.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Smartphone application (CRADLE)
- What this could lead to
- If successful, this app could help parents and doctors spot early signs of eye cancer in children using a smartphone, leading to faster diagnosis.
- What could go wrong
- The study was terminated with only 1 participant, so we have very little data. The app may not be accurate enough to replace standard exams, and results may not apply to all children.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
1 person
The number who actually took part.
- Started
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Mar 2018
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
Up to 7 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria - Stratum I: * Patient has been diagnosed with congenital or infantile cataracts, congenital glaucoma, or retinoblastoma, and is scheduled for a visit with an ophthalmologist at St. Jude Children's Research Hospital or University of Tennessee Hamilton Eye Institute. * Patient with retinoblastoma is newly diagnosed, or has received \< 2 cycles of chemoreductive therapy, and has not undergone enucleation. * Patient with cataracts or glaucoma has not received any prior therapy. Inclusion Criteria - Stratum II: * Patient without prior diagnosis has been referred for ophthalmological evaluation, including leukocoria or other conditions. Inclusion Criteria - Stratum III: * Patient with retinoblastoma undergoing ocular salvage treatment. Exclusion Criteria * Prior treatment for cataracts or glaucoma * Inability or unwillingness of research participant or legal guardian to consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
St. Jude Children's Research Hospital
Memphis, Tennessee, 38105-2794, United States
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