N/A
N=25
Measurement of Refractive SE Following Implantation of LS313 MF30 IOL
Refractive Errors
Bottom Line
View on ClinicalTrials.gov: NCT03292614 ↗Enrolled (actual)
25
Serious AEs
0.0%
Results posted
Sep 2019
Primary outcome: Primary: Evaluation of the Most Precise Method for Measuring Post-operative Refraction Following Implantation of the Asymmetric Multifocal LS-313 MF30 — 0.36; 0.27; -0.81; -0.78 diopter
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Measurements of the postoperative refraction (Diagnostic_test)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Dietrich-Bonhoeffer-Klinikum
- Primary completion
- Jan 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Evaluation of the Most Precise Method for Measuring Post-operative Refraction Following Implantation of the Asymmetric Multifocal LS-313 MF30 |
0.36; 0.27; -0.81; -0.78; -0.73; -0.76 | — |
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 different Autorefractor Keratometers with the subjective measurements for distance and near.
Eligibility Criteria
Inclusion Criteria
Patients after cataract surgery with implantation of the MICS-IOL LS-313 MF30 postoperative clear cornea willing to participate in the study
Exclusion Criteria
significant corneal opacities, history of keratoplasty, Anterior capsule phimosis, posterior capsular opacification if patients refuse Nd:YAG laser treatment of the secondary cataract
Data sourced from ClinicalTrials.gov (NCT03292614). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.