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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON27770

Enrollment

Registered

2012-01-26

Start date

2012-02-01

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glistening in hydrophobic biomaterial Posterior Capsule Opacification Bioadhesion Biocompatibility Intraocular lens stability

Interventions

1. Standard cataract surgery

2. Standard follow-up (slit lamp examination, clinical outcomes, visual acuity testing).

Eligibility

Inclusion criteria

Inclusion criteria: Patients requiring a cataract surgery.

Exclusion criteria

Exclusion criteria: 1. Younger than 21 years old; 2. Informed consent not signed.

Design outcomes

Primary

Measure	Time frame
1. Glistening evaluation; 2. PCO rate; 3. IOL stability.	—

Secondary

Measure	Time frame
1. No adverse events; 2. Surgical facility.	—

Contacts

Public ContactP. Sempoux

Rue Tilleux 38

psempoux@hotmail.com081/31.03.01

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)