Overview
Trial Comparing Two Carboplatin Doses in Groups C and D Intraocular Retinoblastoma
Status:
Unknown status
Unknown status
Trial end date:
2012-04-01
2012-04-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to determine whether an increase in the dose of carboplatin in treatment of advanced intraocular (group C and D) retinoblastoma helps in avoiding radiotherapy and improves the rate of globe salvage.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
All India Institute of Medical Sciences, New DelhiCollaborator:
Council of Scientific and Industrial Research, IndiaTreatments:
Carboplatin
Criteria
Inclusion Criteria:- All new cases of retinoblastoma with group C or D tumor as per the ICRB (International
classification of retinoblastoma, Table 2) that present at Rajendra Prasad Centre for
Ophthalmic Sciences over first 2 years of the study period
Exclusion Criteria:
- Biomicroscopic evidence of iris neovascularization
- Neovascular glaucoma
- Tumor invasion into the anterior chamber, iris, optic nerve, choroid, or extraocular
tissues as documented by clinical, ultrasonographic, and neuroimaging modalities.
- Systemic exclusion criteria include:
- evidence of systemic metastasis
- prior chemotherapy
- prior treatment for retinoblastoma, or
- inadequate renal or hepatic function