This study wants to compare between two types of implants in enucleation. Both of them are made from porous polyethylene but have different fabricating techniques. The investigators chose an exposure rate as a main outcome because the investigators think it is the most important outcome for the surgeons. The study hypothesis is: Is the exposure rate of a local-made polyethylene orbital implant the same as an imported one?
Sample size assessment * The sample size was calculated by using an equivalence formula. From a literature and our own experiences, the success rate for Medpor and 3DP were 92% and 94% respectively, the difference (D) of the success rate between two groups was 10% and assuming a 15% of drop out rate. * Then allocation sequence was generated by a computerized program, using block of six with varying block size. Data management * All definition of data, recruiting techniques, data collection techniques and data management flow were mentioned in the SOP. * After double entry technique, each case record form from each site will be sent via DataFax system to the data center at Center of Excellence for Biomedical and Public Health Informatics (BIOPHICS), Thailand. * Then data will be validated, analyzed and reported by staff at BIOPHICS. Plan for missing data * by adding a drop out rate to the sample size calculation. * by choosing the right patients. Actually, Thai patients have good co-operation especially in surgical research. Statistical analysis \- Intention to treat and per protocol model would be used to see the difference between two types of implants in this project.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
105
Mettapracharak Eye Center, Mettapracharak (Wat Rai Khing) Hospital
Sam Phran, Changwat Nakhon Pathom, Thailand
Exposure rate
Exposure was defined as the separation of tissue over the anterior surface of an implant.
Time frame: From date of surgery until the date of first exposure, assessed up to 12 months
Infection rate
Infection was defined as the presence of pus or abscess at or around an implant. It can be diagnosed clinically or confirmed by the histopathology report after explantation.
Time frame: From date of surgery until the date of first infection, assessed up to 12 months
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