Influence of multifocal intraocular lens on glaucoma diagnostic tests

Completed

• Conditions: implants; Multifocal intraocular lens; 10018307

• Registration Number: NL-OMON40755
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 15

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.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>FDT: number of abnormal test locations;<br /><br>OCT: thickness of the retinal nerve fibre layer (RNFL) and the retinal ganglion<br /><br>cell layer (RGCL);<br /><br>GDx: the nerve fibre index </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Not applicable.</p><br>