Clinical Trials Logo

Retinoblastoma clinical trials

View clinical trials related to Retinoblastoma.

Filter by:
  • Not yet recruiting  
  • Page 1

NCT ID: NCT05028270 Not yet recruiting - Retinoblastoma Clinical Trials

Treatment of Intraocular Retinoblastoma

Start date: June 20, 2022
Phase:
Study type: Observational

This study compares the effects of balloon technology and microcatheter technology on the eye protection rate of neuroblastoma

NCT ID: NCT04344652 Not yet recruiting - Retinoblastoma Clinical Trials

Photoscreening for Retinoblastoma

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

Retinoblastoma is the most common pediatric eye malignancy and manifests between 1 and 5 years of age. The tumor is most often diagnosed by leukocoria ( white reflex in the pupil). There is often a significant delay in diagnosis and early diagnosis enables good life prognosis and better vision outcome.There is currently not a standardized screening protocol for detection of retinoblastoma. Vision screening methods are recommended for children 3-5 years of age. The investigators are attempting to use instrument based screening started from birth to detect leukocoria.

NCT ID: NCT03439397 Not yet recruiting - Retinoblastoma Clinical Trials

RCT of Ballon Technique VS Selective Ophthalmic Artery Infusion For the Retinoblastoma Patients

Start date: March 2018
Phase: N/A
Study type: Interventional

Retinoblastoma is the most common intraocular tumor in children..IAC--Targeted Treatment for Intraocular Retinoblastoma,Is minimally invasive procedure that infuse chemotherapy select into the ophthalmic artery, its can increasing the drug concentration reaching the tumor and reducing systemic toxicity compared with traditional intravenous treatment.: one is Ballon technique , another is selective ophthalmic artery infusion.This study evaluates the difference of Ballon technique and selective ophthalmic artery infusion effect in the treatment of retinoblastoma. Half of participants will receive, Ballon technique while the other half will receive selective ophthalmic artery infusion