Trials / Completed
CompletedNCT02319486
CEV With/Without Periocular Carboplatin Chemotherapy for Extraocular Retinoblastoma
CEV With/Without Periocular Carboplatin Chemotherapy for Nonmetastatic Extraocular Retinoblastoma Carboplatin--A Single Center, Retrospective Study to Evaluate the Efficacy of Carboplatin in Subjects With Retinoblastoma
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Sun Yat-sen University · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
This study will evaluate a uniform chemotherapy protocol for nonmetastatic extraocular retinoblastoma
Detailed description
This study will be a phase 4 open label interventional case series. Patients with retinoblastoma will be receive chemotherapy with or without periocular injections of carboplatin at a dose of 20mg/2 ml. Patients will receive chemotherapy on a monthly basis for a total duration of therapy of 6 months. Patients will be followed for 18 months .
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | carboplatin periocular injection | chemotherapy together with/without 20mg/2ml carboplatin periocular injection |
| DRUG | CEV chemotherapy | vincristine,1.5mg/m2;carboplatin,560mg/ m2;etoposide,150 mg/ m2 |
Timeline
- Start date
- 2009-01-01
- Primary completion
- 2014-04-01
- Completion
- 2014-04-01
- First posted
- 2014-12-18
- Last updated
- 2015-03-30
- Results posted
- 2015-03-30
Source: ClinicalTrials.gov record NCT02319486. Inclusion in this directory is not an endorsement.