Studying Health Outcomes After Treatment in Patients With Retinoblastoma

Recruiting Observational Study
Retinoblastoma Cancer Survivor Biological Sibling Intraocular Retinoblastoma Unilateral Retinoblastoma
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Sex
Any
Study type
Observational
Participants needed
900 (estimated)
Sponsor
Vanderbilt-Ingram Cancer Center · Other
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About This Trial
This trial studies health outcomes after treatment in patients with retinoblastoma. Gathering health information over time from patients and family members through vision assessments, samples of tissue and saliva, and questionnaires may help doctors learn more about what causes retinoblastoma, identify long-term health outcomes for patients with retinoblastoma, and find out which therapies may be …
Trial Locations
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Eligibility Criteria
* Unilateral or bilateral intraocular retinoblastoma * Diagnosis between the ages of 0 - 17.99 years * Diagnosis on or after January 1, 2008 * No exclusions based on primary or secondary treatment modalities * Retrospective group patients must be ≥ 6 months post end of treatment at study entry * …
Contacts

Vanderbilt-Ingram Service for Timely Access

800-811-8480

cip@vanderbilt.edu

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