Chemotherapy Effect Clinical Trial
Official title:
Choice of Topotecan or Melphalan in Retinoblastoma Patients
The purpose of this study is to evaluate topotecan and melphalan for retinoblastoma patients.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | December 30, 2027 |
Est. primary completion date | December 30, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - diagnosed as retinoblastoma - receiving eyeball-sparing treatment Exclusion Criteria: - disease progression during follow-up |
Country | Name | City | State |
---|---|---|---|
China | Sun Yat-sen University | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Sun Yat-sen University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Eyeball-sparing rate | Eyeball-sparing rate during chemotherapy in retinoblastoma patients | 5 years after chemotherapy | |
Secondary | Side effects | Side effects during and after chemotherapy in retinoblastoma patients | 5 years after chemotherapy |
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