Personalized 3D ocular prosthesis vs Conventional prosthesis
- Conditions
- Post enucleation/evisceration10030046
- Registration Number
- NL-OMON56495
- Lead Sponsor
- Amsterdam UMC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 34
Inclusion Criteria
Age 16 or older
Able to understand the study information and instructions
Patients already using an ocular prosthesis for at least 6 months
Cases after enucleation, evisceration, or a prosthesis worn over the own blind
eye
Exclusion Criteria
A potential subject who meets any of the following criteria will be excluded
from participation in this study:
Newly eviscerated or enucleated patients
Socket pathology (cyst, infection, exposure, contraction)
Not able to understand the study information and instructions
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method