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OpenTrials
Completed

NCT Number: NCT03935074

Superselective Intra-arterial Chemotherapy Treatment for Retinoblastoma- 5 Year Results From Turkey

Retrospective review of 5-year long term outcomes of superselective intra-arterial chemotherapy treatment in retinoblastoma in a single institute.

The treatment outcomes, globe salvage rates and complications of superselective intra-arterial chemotherapy both for treating naive patients (primary treatment group) and for patients who received systemic chemotherapy previously (secondary treatment group) were evaluated.

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Key information

Age range

5 month–7 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Istanbul University Cerrahpasa School of Medicine Ophthalmology Department

Istanbul, 34098, Turkey (Türkiye)

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients diagnosed with unilateral/bilateral retinoblastoma

Exclusion criteria

  • patients with trilateral retinoblastoma
  • extraoculer involvement
  • patients with blood dyscrasias, bleeding and clotting disorders

Treatment and study plan

intra-arterial administration of melphalan

Drug

Primary outcomes

  1. globe salvage

    Time frame: 2-5 years

    globe salvage rate after superselective intra-arterial chemotherapy treatment for retinoblastoma

Sponsors and collaborators

Lead sponsor

Istanbul University - Cerrahpasa

Other

Registry information

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
May 2, 2019
Registry last updated
May 6, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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