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
| Type | Name | Description |
|---|---|---|
| OTHER | intrastromal corneal ring segments (Keraring) implantation | |
| OTHER | Intrastromal 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.