Skip to content

Visual and refractive outcomes of a hydrophobic monofocal aspheric hydrophobic intraocular lens with C-Loop haptics after cataract surgery.

Visual and refractive outcomes of a hydrophobic monofocal aspheric hydrophobic intraocular lens with C-Loop haptics after cataract surgery. - LUCIA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00029169
Enrollment
55
Registered
2022-05-30
Start date
2022-06-17
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Eyes operated by cararact surgery.

Interventions

Group 1: Patients 50 years of age or older who will undergo cataract surgery with phacoemulsification and will be implanted with the lens under study (LUCIA 621P IOL).

Sponsors

Doctor, investigateur coordinateur and Promoter's representative of OFTALVIST (Oftalmología Vistahermosa, SL)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients 50 years of age or older who are going to undergo cataract surgery with phacoemulsification. 2. Patient who signs the informed consent form. 3. Regular corneal astigmatism up to 1.0D. 4. LIO power between 0D and 34D. 5. Patients to be implanted with the lens under study (LUCIA 621P LIO) during cataract surgery.

Exclusion criteria

Exclusion criteria: 1. Patients who do not provide informed consent. 2. Patients who do not understand the study procedure. 3. Irregular cornea (e.g. keratoconus). 4. Previous corneal refractive surgery. 5. Ocular abnormalities or pathologies that could reduce visual function or LIO stability (e.g. severe amblyopia or macular degeneration).

Design outcomes

Primary

MeasureTime frame
The refractive and visual outcomes of patients undergoing cataract surgery with the implantation of hydrophobic monofocal aspheric hydrophobic intraocular lens (LIO) with C-loop LUCIA 621P haptics will be analyzed. The results obtained are intended to add more information to the published literature on this LIO.

Secondary

MeasureTime frame
Evaluation of the patient's visual acuity, ocular aberrations, contrast sensitivity and subject satisfaction.

Countries

Spain

Contacts

Public ContactMaria Cobo

Study coordinator

maria.cobo@oftalvist.es+34963513304

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026