Postoperative Complications Clinical Trial
Official title:
Post-enucleation Socket Syndrome Study (PESSS): Part 1 - Three Dimensional Volumetric Assessment of Anophthalmic Sockets With the New Multi-detector Computed Tomographic Technology
Verified date | May 2010 |
Source | Singapore National Eye Centre |
Contact | n/a |
Is FDA regulated | No |
Health authority | Singapore: Health Sciences Authority |
Study type | Observational |
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 underlying reasons include the lack of accurate pre-operative volumetric
assessment of the anophthalmic socket, leading to either under or over estimation of the
orbital implant required and the shifting in orbital and periocular structures that may
occur post enucleation. Conventional imaging studies (computed tomography and magnetic
resonance imaging) have been used to study the anatomy of anophthalmic sockets, but there
are several drawbacks such as poor image quality for detailed volumetric assessment, long
exposure time with possible motion artifact and etc. The new multi-detector computed
tomographic technology is the latest advance in diagnostic radiology that allows rapid high
resolution images to be obtained for three dimensional reconstruction and volumetric
assessment. This new imaging modality will contribute greatly to the understanding of PESS
and the surgical planning of anophthalmic sockets reconstruction.
This is a pilot study aiming to collect clinical data on the volumetric and structural
changes in PESS. The information obtained will:
1. allow more accurate volume estimation of the primary orbital implants prior to
enucleation surgeries, thus minimize the development of PESS;
2. evaluate the volumetric & structural anomalies that constitute PESS
3. be used for the development of a new customized secondary orbital implant to manage
superior sulcus deformity in PESS.
Status | Completed |
Enrollment | 10 |
Est. completion date | January 2010 |
Est. primary completion date | January 2010 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: - 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 Criteria: - 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 |
Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Singapore | Singapore Eye Research Institute | Singapore |
Lead Sponsor | Collaborator |
---|---|
Singapore National Eye Centre |
Singapore,
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* Note: There are 22 references in all — Click here to view all references
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