Clinical Trials Directory

Trials / Unknown

UnknownNCT01647373

Axial Length Change in Eyes Treated by Silicone Sponge Scleral Buckling

Axial Length Change in Eyes Treated by Silicone Sponge Scleral Buckling.

Status
Unknown
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Meir Medical Center · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Timeline

Start date
2013-07-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2012-07-23
Last updated
2013-06-12

Locations

2 sites across 1 country: Israel

Source: ClinicalTrials.gov record NCT01647373. Inclusion in this directory is not an endorsement.

Axial Length Change in Eyes Treated by Silicone Sponge Scleral Buckling (NCT01647373) · Clinical Trials Directory