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Clinical Trials/DRKS00010108
DRKS00010108
Completed
Not Applicable

Observational study to assess clinical outcomes and patient satisfaction after multifocal IOL implantation

Optana GmbH0 sites28 target enrollmentMarch 2, 2016
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Conditionspatient satisfaction after implantation of a multi-focal IO

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
patient satisfaction after implantation of a multi-focal IO
Sponsor
Optana GmbH
Enrollment
28
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 2, 2016
End Date
June 15, 2016
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Optana GmbH

Eligibility Criteria

Inclusion Criteria

  • •Patients must have read, understood and signed the Patient Information (Informed Consent Form)
  • •Patients that underwent uneventful refractive surgery (LASIK, PRK) after cataract surgery can be included
  • •Only patients that underwent uneventful cataract surgery with a bilateral implantation of multifocal IO

Exclusion Criteria

  • •Existing posterior capsule opacity (PCO) at the day of study examination
  • •The time between the surgeries of both eyes is maximum 3 months
  • •Clinically significant glaucoma
  • •Clinically significant macular degeneration, clinically significant macular edema or proliferative diabetic retinopathy
  • •Patients with keratoconus or keratectasia
  • •Patients who are pregnant or nursing
  • •Abnormal examination results from slit lamp, fundus examination or IOL Master, topography, age related changes are acceptable
  • •Patients who do not give informed consent

Outcomes

Primary Outcomes

Not specified

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