Clinical Trials Directory

Trials / Completed

CompletedNCT03193411

Visumax Femtolasik Versus Moria M2 Microkeratome in Myopia

Visumax Femtolasik Versus Moria M2 Microkeratome in Mild to Moderate Myopia: Efficacy, Safety, Predictability, Aberrometric Changes and Flap Thickness Predictability

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Dar Al Shifa Hospital · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

this is an interventional prospective clinical study which was conducted to evaluate the efficacy, safety, predictability, ocular aberrations, and flap thickness predictability of Visumax femtosecond laser (FSL) compared to Moria M2 microkeratome (MK) in mild to moderate myopia.

Detailed description

This study included 60 eyes who were divided into two groups. Thirty eyes in group (I) in which the flap was created with Visumax FSL, while in group II (30 eyes) the Moria M2 MK was used. Keratometric, refractive, and aberrometric measurements were compared preoperatively and 3 months postoperatively. The intraoperative subtraction pachymetry (the SP 100 Handy pachymeter (Tomey, Nagoya, Japan) was used for preoperative pachymetry and flap thickness measurement.

Conditions

Interventions

TypeNameDescription
DEVICEVisumax femtosecond laser
DEVICEMoria M2 microkeratome (MK)

Timeline

Start date
2014-01-01
Primary completion
2014-05-29
Completion
2014-06-01
First posted
2017-06-20
Last updated
2017-06-20

Source: ClinicalTrials.gov record NCT03193411. Inclusion in this directory is not an endorsement.