Understanding the incidence and outcomes of trilateral retinoblastoma
Official title: Global Survey of Trilateral Retinoblastoma: Incidence and Outcomes
Run by Amsterdam UMC, location VUmc · NCT06367530 · Data updated 2026-11-12
This study looks at how common trilateral retinoblastoma is and how well patients survive, comparing data from different countries to see if there are differences based on income levels.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 4351 (estimated) |
| Sponsor | Amsterdam UMC, location VUmc Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Amsterdam, North Holland) |
| Status | Recruiting |
| Started | January 1, 2024 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2029 |
| Registry record updated | April 16, 2024 |
| Trial ID | NCT06367530 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with retinoblastoma.
✕Probably not a fit
Patients who do not have a diagnosis of retinoblastoma will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to investigate the incidence and survival rates of trilateral retinoblastoma among patients diagnosed with retinoblastoma globally. It will include data from various treatment centers over a specified period, focusing on the differences in incidence between high-income and low-income countries. The study will follow a prospective cohort design, adhering to established reporting guidelines to ensure accuracy and transparency. Data will be collected on the location of the tumors, treatment received, and survival outcomes to enhance understanding of this condition.
Why it matters
Potential benefit: If successful, this study could lead to improved health practices and outcomes for retinoblastoma patients, particularly in low-income regions.
How similar studies have gone: Previous studies on retinoblastoma have shown success in understanding its global incidence and outcomes, making this approach both relevant and necessary.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients diagnosed with retinoblastoma Exclusion Criteria: * none
Where it's running
-
Amsterdam UMC
Amsterdam, North Holland, Netherlands Recruiting
Study contacts
- Principal investigator: Marcus de Jong, MD PhD — Amsterdam UMC
- Study coordinator: Marcus C de Jong, MD PhD
- Email: mc.dejong@amsterdamumc.nl
- Phone: +31(0)20-4443047
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Chemotherapy for high-risk retinoblastoma after eye removal
This study is testing if giving chemotherapy after removing the eye can help prevent high-risk retinoblastoma from coming back in children with Stage I disease.
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This study is trying to see if collecting eye fluid from children with retinoblastoma can help find important markers for better treatment and understanding of the disease.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.