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Clinical Trials/NL-OMON40755
NL-OMON40755
Completed
Not Applicable

Influence of multifocal intraocular lens on glaucoma diagnostic tests - multifocal intraocular lens and glaucoma tests

niversitair Medisch Centrum Groningen0 sites15 target enrollmentTBD
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ConditionsimplantsMultifocal intraocular lens10018307

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
implants
Sponsor
niversitair Medisch Centrum Groningen
Enrollment
15
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • •\- Patients implanted with a MFIOL aged between 18 an 70, who are able and willing to participate in this study.
  • •\- Postoperative period of at least 3 months.
  • •\- One eye will be randomly chosen and tested with the exception of the FDT. This device can only perform the test if both eyes are analysed.

Exclusion Criteria

  • •\- Best correct visual acuity (BCVA) of \<0\.8 or \<0\.67 when aged above 50\.
  • •\- Refractive error \>±5D or a cylinder of \>±2\.5D.
  • •\- Intra ocular pressure (IOP) of \>22mmHg.
  • •\- Optic nerve abnormalities indicating glaucoma
  • •\- Repeatable VF\-defects detected with perimetry (not explained by the MFIOL in patients)
  • •\- History or current serious eye disease, trauma or surgery.

Outcomes

Primary Outcomes

Not specified

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