Sutures in Orbital Implants in Retinoblastoma Patients

The purpose of this study is to evaluate different sutures for orbital implants in retinoblastoma patients.

Completed

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Key information

Conditions

Surgery--Complications Eye Diseases Eye Diseases, Hereditary Eye Neoplasms Neoplasms Neoplasms by Histologic Type Neoplasms by Site Neoplasms, Germ Cell and Embryonal Neoplasms, Glandular and Epithelial Neoplasms, Nerve Tissue Neoplasms, Neuroepithelial Neuroectodermal Tumors Retinal Diseases Retinal Neoplasms Retinoblastoma Retinoblastoma Bilateral

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

To evaluate the effectiveness and complications of 4-0 and 5-0 sutures for orbital implants in retinoblastoma patients.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

diagnosed as retinoblastoma
enucleation and orbital implantation in the same surgery

Exclusion criteria

death during follow-up

Treatment and study plan

5-0 suture

Procedure

5-0 suture administration during surgery

Other names: 5-0 suture administration

4-0 suture

Procedure

4-0 suture administration during surgery

Other names: 4-0 suture administration

Primary outcomes

Rate of participants with complications

Time frame: 2 year after surgery

complications, such as orbital implant exposure in the follow-up visit

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Registry information

Official study title

Choice of Sutures in Orbital Implants in Retinoblastoma Patients

Important dates

Study start: 2015
Primary completion: 2017
Study completion: 2020
First posted: May 12, 2020
Registry last updated: Jun 15, 2021

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.

Published trials that share one or more normalized conditions with this study.

Completed