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A Prospective Observational Case Series of a Four-ring-haptic Acrylic One-piece IOL

Completed
Conditions
Cataract
Registration Number
NCT01244373
Lead Sponsor
General Hospital Linz
Brief Summary

To describe biocompatibility, postoperative results and complications after implantation of the Corneal Quatrix Evolutive (Corneal, Croma, Austria) intraocular lens, a hydrophilic acrylic intraocular lens (IOL) with 4-haptic design and 360° sharp optic edge.

Detailed Description

In this prospective case series the Corneal Quatrix Evolutive IOL was implanted in 14 eyes of nine patients with senile cortico-nuclear cataract. A standardized surgical technique and post-operative regimen were applied. Six months postoperatively best corrected visual acuity (BCVA), refraction and complications (especially) posterior capsule opacification (PCO) were analysed.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
9
Inclusion Criteria

Patients with senile cortico-nuclear cataracts without previous intraocular surgery

Exclusion Criteria
  • Dilated pupil size of < 6 mm
  • long-term anti-inflammatory treatment
  • previous history of intraocular surgery
  • previous history of corneal endothelial damage
  • previous history of ocular trauma
  • traumatic cataract
  • history of uveitis
  • diabetic retinopathy
  • advanced macular degeneration

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Best-corrected visual acuity (BCVA)Six months

The best-corrected visual acuity is assessed with glasses after cataract operation

Secondary Outcome Measures
NameTimeMethod
Posterior capsule opacificationSix months

The posterior capsule opacification is assessed by slit lamp examination and subjective grading

Trial Locations

Locations (1)

Department of ophthalmology, General Hospital Linz

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Linz, Upper Austria, Austria

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