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
| Type | Name | Description |
|---|---|---|
| DEVICE | Visumax femtosecond laser | |
| DEVICE | Moria 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.