Status:
COMPLETED
Post Enucleation Socket Syndrome Study
Lead Sponsor:
Singapore National Eye Centre
Conditions:
Eye Enucleation
Orbit Surgery
Eligibility:
All Genders
21+ years
Brief Summary
Superior sulcus deformity in post-enucleation socket syndrome (PESS) may pose a significant cosmetic blemish after enucleation surgery despite apparently adequate orbital volume replacement. The under...
Detailed Description
Purpose: Primary aim: Three dimensional volumetric assessment of the changes in orbital soft tissues in patient with post-enucleation socket syndrome, using the new 16-slice multi-detector computed ...
Eligibility Criteria
Inclusion
- Patient who underwent :
- standard uncomplicated enucleation,
- with primary hydroxyapatite or MEDPORE implant of size 20mm diameter or larger well placed within the posterior Tenon's space,
- and re-suturing of the four recti muscles anterior to the equator,
- Aged 21 and above
- In good general health
Exclusion
- Other types of orbital implant or implant size smaller than 20mm
- History of any disorders or surgery of the orbits: e.g. orbital trauma, repair of orbital fracture, orbital tumors, thyroid eye disease, orbital inflammatory disease, orbital irradiation
- History of any disorders or surgery of the extraocular muscles: e.g. myopathy, strabismus surgery
- History of any disorders or surgery of the eyelids: e.g. congenital ptosis, Horner's syndrome, ptosis surgery
- Pregnancy
Key Trial Info
Start Date :
March 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 1 2010
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT00347282
Start Date
March 1 2006
End Date
January 1 2010
Last Update
May 12 2010
Active Locations (1)
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1
Singapore Eye Research Institute
Singapore, Singapore, 168751