Photoscreening for Retinoblastoma
Primary Purpose
Retinoblastoma
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Photoscreening -
Sponsored by
About this trial
This is an interventional diagnostic trial for Retinoblastoma
Eligibility Criteria
Inclusion Criteria:
- Age birth to 10 years
- Informed consent given by parent or legal guardian
Exclusion Criteria:
- None
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Photoscreening
Arm Description
Photoscreening of patients 0 to 10 years of age
Outcomes
Primary Outcome Measures
Reliability to detect leukocoria
Testing the reliability of the app to detect leukocoria with good sensitivity and specificity
Secondary Outcome Measures
Full Information
NCT ID
NCT04344652
First Posted
April 9, 2020
Last Updated
April 13, 2020
Sponsor
Phoenix Children's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04344652
Brief Title
Photoscreening for Retinoblastoma
Official Title
Prospective Evaluation of a Smartphone Application, GoCheckKids TM, as a Screening Tool for Leukocoria in the Infant and Pediatric Population
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2020 (Anticipated)
Primary Completion Date
May 31, 2021 (Anticipated)
Study Completion Date
May 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Phoenix Children's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Retinoblastoma is the most common pediatric eye malignancy and manifests between 1 and 5 years of age. The tumor is most often diagnosed by leukocoria ( white reflex in the pupil). There is often a significant delay in diagnosis and early diagnosis enables good life prognosis and better vision outcome.There is currently not a standardized screening protocol for detection of retinoblastoma. Vision screening methods are recommended for children 3-5 years of age. The investigators are attempting to use instrument based screening started from birth to detect leukocoria.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinoblastoma
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single visit cross sectional prospective study
Masking
None (Open Label)
Allocation
N/A
Enrollment
76 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Photoscreening
Arm Type
Experimental
Arm Description
Photoscreening of patients 0 to 10 years of age
Intervention Type
Device
Intervention Name(s)
Photoscreening -
Intervention Description
external picture taken with a an phone based app
Primary Outcome Measure Information:
Title
Reliability to detect leukocoria
Description
Testing the reliability of the app to detect leukocoria with good sensitivity and specificity
Time Frame
1 year
10. Eligibility
Sex
All
Gender Based
Yes
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age birth to 10 years
Informed consent given by parent or legal guardian
Exclusion Criteria:
None
12. IPD Sharing Statement
Learn more about this trial
Photoscreening for Retinoblastoma
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