Sutures in Orbital Implants in Retinoblastoma Patients

Choice of Sutures in Orbital Implants in Retinoblastoma Patients

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04383860

Enrollment

132

Registered

2020-05-12

Start date

2015-01-01

Completion date

2020-07-01

Last updated

2021-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retinoblastoma Bilateral, Surgery--Complications

Keywords

Retinoblastoma, suture, complications

Brief summary

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

Detailed description

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

Interventions

PROCEDURE5-0 suture

5-0 suture administration during surgery

PROCEDURE4-0 suture

4-0 suture administration during surgery

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* diagnosed as retinoblastoma * enucleation and orbital implantation in the same surgery

Exclusion criteria

* death during follow-up

Design outcomes

Primary

Measure	Time frame	Description
Rate of participants with complications	2 year after surgery	complications, such as orbital implant exposure in the follow-up visit

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026