Evaluation of the performance and the stability of an intraocular lens.

• Conditions: Glistening in hydrophobic biomaterialPosterior Capsule OpacificationBioadhesionBiocompatibilityIntraocular lens stability

• Registration Number: NL-OMON27770
• Lead Sponsor: /A

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 50

Inclusion Criteria

Patients requiring a cataract surgery.

Exclusion Criteria

1. Younger than 21 years old;

2. Informed consent not signed.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
1. Glistening evaluation;<br /><br>2. PCO rate;<br /><br>3. IOL stability.

Secondary Outcome Measures

Name	Time	Method
1. No adverse events;<br /><br>2. Surgical facility.<br>