Status:

COMPLETED

Measurement of Refractive SE Following Implantation of LS313 MF30 IOL

Lead Sponsor:

Dietrich-Bonhoeffer-Klinikum

Conditions:

Refractive Errors

Eligibility:

All Genders

18+ years

Brief Summary

This Study determines the most precise method for measuring post-operative refraction following implantation of the asymmetric multifocal LS-313 MF30 comparing the results of Refraction of the differe...

Detailed Description

This is a post market study without invasive interventions. The patients have been treated with cataract surgery and MIOL Implantation at least 3 months ago. They will be invited for only one follow u...

Eligibility Criteria

Inclusion

  • Patients after cataract surgery with implantation of the MICS-IOL LS-313 MF30 postoperative clear cornea willing to participate in the study

Exclusion

  • significant corneal opacities, history of keratoplasty, Anterior capsule phimosis, posterior capsular opacification if patients refuse Nd:YAG laser treatment of the secondary cataract

Key Trial Info

Start Date :

June 1 2017

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

June 1 2019

Estimated Enrollment :

25 Patients enrolled

Trial Details

Trial ID

NCT03292614

Start Date

June 1 2017

End Date

June 1 2019

Last Update

September 26 2019

Active Locations (1)

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Dietrich-Bonhoeffer-Klinikum

Neubrandenburg, Mecklenburg-Vorpommern, Germany, 17036