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Comparison of Two Different Intraocular Lenses Implanted With Yamane Technique

J

Johannes Kepler University of Linz

Status

Enrolling

Conditions

Secondary Cataract Surgery
Aphakia
Complicated Cataract Surgery

Treatments

Device: MS-39
Device: Casia-2
Diagnostic Test: Biomicroscopy
Device: OSIRIS
Device: IOL Master 700
Device: Autorefractor
Diagnostic Test: Subjective Refraction

Study type

Observational

Funder types

Other

Identifiers

NCT05912829
KUK-Ophthalmology-012

Details and patient eligibility

About

In case of instability or rupture of capsular bag occurs during cataract surgery, Yamane technique is one of the options to fix intracocularlens' haptics. Yamane technique uses a double-needle technique that seamlessly fixes the haptics intrascleral by creating a scleral tunnel.

Aberrations, IOL tilting or even dislocations might occur and influence the final outcome of IOL implantation.

The aim of this study is the evaluation of the postoperative tilt of Kowa PU6AS using Yamane technique. Furthermore of the corrected and uncorrected visual acuity and the anterior chamber depth are being developed.

Full description

During uncomplicated cataract surgery, an intraocular lens (IOL) is implanted into the patient's capsular bag. If increased instability or rupture of this capsular bag occurs due to aggravated intraoperative conditions or IOL dislocation, several options are available to the surgeon to correct the aphakia, all characterized by their respective advantages and disadvantages, but with no clear superiority of any one method.

The popular Yamane technique, or "flanged IOL fixation", uses a double-needle technique that seamlessly fixes the haptics intrascleral by creating a scleral tunnel using two 30-gauge needles.

Examples of lenses used for this purpose are the TECNIS ZA9003 (Johnson&Johnson, USA) and the Kowa PU6AS (Kowa, Japan). Another approach is the Carlevale FIL-SSF IOL (Soleko, Italy), which was developed specifically for use in aphakia with lack of capsular stability.

All types of implantation are not immune to aberrations, tilting or even dislocation. Many factors influence the final outcome of IOL implantation, be it the optimal choice of intraocular lens power, the surgeon's experience regarding fixation in more challenging eyes, or individual anatomical conditions. As part of quality assurance, an evaluation of monthly and six-monthly data will now be performed. The aim of this study is the evaluation of the postoperative tilt of the Kowa PU6AS in Yamane technique, as well as the evaluation of the corrected and uncorrected visual acuity and the anterior chamber depth within the clinical quality management.

Enrollment

50 estimated patients

Sex

All

Ages

21 to 110 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Minimum age: 21 Years
  • planned or performed lens implantation using the Kowa PU6AS or the Johnson & Johnson ZA9003 using the Yamane technique
  • signed patient consent form

Exclusion criteria

  • best corrected visual acuity >0.1 (Snellen)
  • pregnancy

Trial design

50 participants in 2 patient groups

Kowa Group
Description:
Patients who had a Kowa lens implanted using the Yamane technique
Treatment:
Diagnostic Test: Subjective Refraction
Device: OSIRIS
Device: IOL Master 700
Device: Autorefractor
Device: Casia-2
Diagnostic Test: Biomicroscopy
Device: MS-39
Johnson
Description:
Patients who had the ZA9003 (J\&J) lens implanted using the Yamane technique
Treatment:
Diagnostic Test: Subjective Refraction
Device: OSIRIS
Device: IOL Master 700
Device: Autorefractor
Device: Casia-2
Diagnostic Test: Biomicroscopy
Device: MS-39

Trial contacts and locations

2

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Central trial contact

Christina Silber, MSc; Nino Hirnschall, MD

Data sourced from clinicaltrials.gov

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