Comperative Trial Between an Accommodative Iol and Monofocal Iol

A Randomized Single Blind Comparative Study of the Acuity's C-Well Accommodating Intra Occular Lens (AIOL) Against Alcon's Acrysof

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00604305

Enrollment

Registered

2008-01-30

Start date

2008-03-31

Completion date

2012-12-31

Last updated

2012-06-12

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

Conditions

CATARACT SURGERY

Brief summary

a comparison of two intraocular lenses in regard of accommodative power.

Detailed description

A new accommodating IOL (Acuity Ltd, Israel) will be compared with Alcon's Acrysof for 1 year for visual acuity and distance and near best corrected visual acuity.

Interventions

DEVICEAcrysof

Monofocal IOL

DEVICEAcuity's AIOL

Accommodating IOL

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

30 Years to 65 Years

Healthy volunteers

Inclusion criteria

* Age between 30 and 65 * Required cataract operation in one or both eyes * BCVA potetial at least 20/30 * Clear intraoccular media * Willing to participate in study as evidenced by signing a written Informed Consent

Exclusion criteria

Main * Prior surgery at the selected eye * No light perception or poor potential for improvement * Phacodonesis and damaged zonules * Pupil size at least 6 mm. * History of uveitis * Macular disease decreasing vision below 20/30 * Amblyopia * Axial length shorter than 21 mm and longer than 25 mm

Design outcomes

Primary

Measure	Time frame
distance and near visual acuity	1 year

Secondary

Measure	Time frame
centration pco	1 year

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026