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NCT04383860 Clinical Trial

Sutures in Orbital Implants in Retinoblastoma Patients

Surgery--Complications Clinical Trial

Official title:
Choice of Sutures in Orbital Implants in Retinoblastoma Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04383860
Other study ID # 202001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2015
Est. completion date July 1, 2020

Study information
Verified date June 2021
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 132
Est. completion date July 1, 2020
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - diagnosed as retinoblastoma - enucleation and orbital implantation in the same surgery Exclusion Criteria: - death during follow-up

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• 5-0 suture
5-0 suture administration during surgery
• 4-0 suture
4-0 suture administration during surgery

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Sun Yat-sen University

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