MedTrace Logo

Evaluation of Stability After Implantation of Two Different Lens Models: FEMTIS-study

NCT03152500 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2018-05-02

No results posted yet for this study

Summary

In this study the investigators will investigate the stability of lens position and the visual outcome after implantation of the new FEMTIS-IOL using FLACS capsulotomy compared to conventional placement of the IOL in the capsular bag. So far, there are no published studies using the FEMTIS-IOL. Therefore, the investigators will perform this randomized control trial.

Conditions

  • Cataract

Interventions

DEVICE

FEMTIS 313G IOL

Haptic design that enclaves the capsulorrhexis

DEVICE

Acrysof SN60WF IOL

IOL in the bag

Sponsors & Collaborators

  • Oculentis

    collaborator UNKNOWN

  • Maastricht University Medical Center

    lead OTHER

Principal Investigators

  • Rudy Nuijts, MD PhD · University Eye Clinic Maastricht, Maastricht University Medical Centre

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-01-01
Primary Completion
2017-09-30
Completion
2017-10-30

Countries

  • Netherlands

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03152500 on ClinicalTrials.gov