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Observation of Rotation of an Intraocular Lens

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Medical University of Vienna

Status

Completed

Conditions

Cataract

Treatments

Procedure: cataract surgery

Study type

Observational

Funder types

Other

Identifiers

NCT02208232
EK Nr: 1267/2012

Details and patient eligibility

About

The purpose of this study is to assess the axial IOL rotation after surgery with an MC 6125 AS IOL.

At the end of surgery the orientation of the IOL is documented with a short video clip via the operating microscope unit. Follow-up examinations are performed 1 hour, 1 week and 6 months after surgery. Rotational stability of the IOL is assessed using retroillumination images with a method to avoid bias from cyclorotation or head tilt.

Enrollment

100 patients

Sex

All

Ages

40 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Uni or bilateral age-related cataract necessitating phacoemulsification extraction and posterior IOL implantation

Exclusion criteria

  • Preceding ocular surgery or trauma
  • Recurrent intraocular inflammation of unknown etiology
  • Uncontrolled glaucoma
  • Uncontrolled systemic or ocular disease
  • Blind fellow eye
  • Microphthalmus
  • Corneal abnormality
  • History of uveitis/iritis
  • Iris neovascularization
  • Pseudoexfoliation
  • Proliferative diabetic retinopathy

Trial design

100 participants in 1 patient group

MC 6125 AS IOL
Description:
cataract surgery with implantation of intraocular lens MC 6125 AS in one eye
Treatment:
Procedure: cataract surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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