ClinicalTrials.Veeva

Menu

Axial Length Change in Eyes Treated by Silicone Sponge Scleral Buckling

Clalit Health Services logo

Clalit Health Services

Status

Unknown

Conditions

Rhegmatogenous Retinal Detachment

Study type

Observational

Funder types

Other

Identifiers

NCT01647373
0125-12

Details and patient eligibility

About

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.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients at least 6 months after succesful retinal detachment surgery
  • with silicone sponge scleral buckling
  • currently attached
  • with IOL Master pre-surgery Axial Length measurement

Exclusion criteria

  • 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

Trial contacts and locations

2

Loading...

Central trial contact

Alexander Rubowitz, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems