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RecruitingNCT05080010

Adjuvant Chemotherapy for High-risk Postenucleation Retinoblastoma

Three Cycles of Adjuvant Chemotherapy for the Patients With High-risk Retinoblastoma After Enucleation: Prospective Study

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
500 (estimated)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the effect of 3 cycles of chemotherapy(CEV) in the treatment of Stage I enucleated retinoblastoma.

Detailed description

This study will be a phase Ⅲ open label interventional case series. Patients with Stage I enucleated retinoblastoma will receive 3 cycles of chemotherapy(CEV) oon a monthly basis. Patients will be followed for 60 months.

Conditions

Interventions

TypeNameDescription
DRUG3 cycles chemotherapyChemotherapy:vincristine,1.5mg/m2;carboplatin,560mg/ m2;etoposide,150 mg/ m2.monthly for the first three months.

Timeline

Start date
2020-11-01
Primary completion
2030-12-31
Completion
2030-12-31
First posted
2021-10-15
Last updated
2021-10-15

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05080010. Inclusion in this directory is not an endorsement.

Adjuvant Chemotherapy for High-risk Postenucleation Retinoblastoma (NCT05080010) · Clinical Trials Directory