Clinical Trials Directory

Trials / Unknown

UnknownNCT01869517

Myoring Versus Keraring Implantation for Keratoconus

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
23 (planned)
Sponsor
Shahid Beheshti University of Medical Sciences · Academic / Other
Sex
All
Age
20 Years – 40 Years
Healthy volunteers

Summary

Various approaches, including surgical and non-surgical management have been proposed for keratoconus. One of the surgical procedures is Intrastromal Corneal Ring implantations that have been designed to achieve refractive readjustment by flattening the cornea. There are different models of Intrastromal Corneal rings available: intrastromal corneal ring segments (ICRS) such as Keraring and intrastromal corneal continuous ring (ICCR) like Myoring. Most studies of these two types of ring implantation outcomes are retrospective case series. Thus, this Randomized Clinical Trial study was designed with the aim of Comparing visual and refractive outcomes and complications of insertion Myoring versus Keraring using Femtosecond laser. Keratoconus patients with compound myopic astigmatism who meet the inclusion criteria will randomly allocated to the Keraring and Myoring groups. Subsequently, the clinical outcomes of two groups will be compared at one,3 and 6 months after surgery.

Conditions

Interventions

TypeNameDescription
OTHERintrastromal corneal ring segments (Keraring) implantation
OTHERIntrastromal corneal continuous ring (Myoring) implantation

Timeline

Start date
2013-05-01
Primary completion
2015-05-01
First posted
2013-06-05
Last updated
2013-06-05

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT01869517. Inclusion in this directory is not an endorsement.