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Clinical results of porous silicone orbital implants

The effect of porous silicone sphere implant

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002189
Enrollment
20
Registered
2017-01-06
Start date
2015-07-27
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Yeungnam University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: It is intended for those who need to evisceration or secondary orbital implants at a hospital participating in the test and those who agreed to this study.

Exclusion criteria

Exclusion criteria: Pregnant women, children / minors

Design outcomes

Primary

MeasureTime frame
implant expose, migration, extrusion, orbital infection and inflammatory reaction—

Secondary

MeasureTime frame
fibrovascularization of implant—

Countries

Korea, Republic of

Contacts

Public ContactJunHyuk Son

Yeungnam University

junhyuk_son@naver.com+82-53-620-3444

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026