A prospective randomised study of the early complication rates of hydroxyapatite versus Medpor orbital implant in the post-enucleation and evisceration socket.
Completed
- Conditions
- Surgery: Orbitant implantsSurgeryOrbitant implants
- Registration Number
- ISRCTN55878769
- Lead Sponsor
- Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
All patient having eyeball removed and having orbital implants inserted at the same operation.
Exclusion Criteria
Patients who are having implants inserted in a secondary procedure.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method