Axial Length Change in Eyes Treated by Silicone Sponge Scleral Buckling
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ClinicalTrials.gov Identifier: NCT01647373
Recruitment Status : Unknown
Verified July 2012 by Meir Medical Center. Recruitment status was: Not yet recruiting
All existing medical literatue regarding axial length (AL) changes after scleral buckling surgery for retinal detachment, descibes changes after solid silicone buckling. In this hospital, the investigators use only silicone sponge buckling, which has different properties and a different buckle profile. there are no studies in the literature describing tha AL changes after sponge buckling, or whether the AL change is less or more than with solid silicone buckles. The investigators wish to determine whether the AL change profile with their silicone sponge is significantly different, and if so, whether this is clinically important in determining the better choice of buckle material to be preferred.
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Ages Eligible for Study:
18 Years to 90 Years (Adult, Senior)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Patients at least 6 months after succesful retinal detachment surgery, with silicone sponge scleral buckling, currently attached, and with IOL Master pre-surgery Axial Length measurement .
Patients at least 6 months after succesful retinal detachment surgery
with silicone sponge scleral buckling
with IOL Master pre-surgery Axial Length measurement
patients with failed surgery and currently detached
patients with vitreos silicone oil tamponade
patients with radial or other non-circumference buckles
patients with unclear media not amenable to IOL Master exam