To study the success rate of evisceration with Hydroxyapatite orbital implant compared with Polymethylmethacrylate orbital implant
Phase 2
- Conditions
- patients who has to undergo evisceration in conditions of endophthalmitis,panophthalmitis,painful blind eye,phthisis bulbi
- Registration Number
- TCTR20181127003
- Lead Sponsor
- Faculty of medicine, Chulalongkorn university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending (Not yet recruiting)
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
-A patient attendind Chulalongkorn hospital who has to undergo evisceration with inclusion criteria of severe corne ulcer, panophthalmitis , endophthalmitis, painful blind eye, phthisis bulbi.
-A patient with more than 15 years of age
Exclusion Criteria
-A patient suspected of orbital mass or carcinoma.
-A patients with severe disfigured orbital bone
-A patient who underwent eyelid surgery or orbital surgery
-A patient with medical conditions that is unable to perform surgery under general anesthesia.
-A patient who undergoes evisceration without orbital implantation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Success rate 2 month Able to put on a prosthesis ,Success rate 2 month Able to put on a prosthesis
- Secondary Outcome Measures
Name Time Method Complication rate 2 month To measure extrusion, exposure rate , Infection rate,Volume, motiity 2 month With hertel exophthalmometry, orbital and prosthesis motility from primary position