Active, not recruitingNCT00639301
Retinoblastoma Survivor Study: Assessment of General Health and Quality of Life
Studying Hereditary retinoblastoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Memorial Sloan Kettering Cancer Center
- Principal Investigator
- Danielle Novetsky Friedman, MDMemorial Sloan Kettering Cancer Center
- Intervention
- Questionnaires(behavioral)
- Enrollment
- 473 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2008 – 2027
Study locations (1)
- Memorial Sloan Kettering Cancer Center, New York, New York, United States
Collaborators
National Cancer Institute (NCI) · St. Jude Children's Research Hospital
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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