Carboplatin Periocular Injection for Retinoblastoma

Status Recruiting

Clinical Trial Summary

This study will evaluate the clinical efficacy of periocular injections of carboplatin together with chemotherapy in the treatment of Retinoblastoma as compared to chemotherapy alone.

Clinical Trial Description

This study will be a phase Ⅲ open label interventional case series. Patients with retinoblastoma will be randomized to receive chemotherapy with or without periocular injections of carboplatin at a dose of 20mg/2 ml. Patients will receive carboplatin periocular on a monthly basis for a total duration of therapy of 6 months. Patients will be followed for 24 months . ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Retinoblastoma

Clinical Trial Details

NCT number	NCT02137928
Study type	Interventional
Source	Sun Yat-sen University
Contact	Huasheng Yang, M.D, PHD
Phone	+8620-87331539
Email	yanghs64@126.com
Status	Recruiting
Phase	Phase 3
Start date	January 2006
Completion date	December 2015

View Details

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