Comperative Trial Between an Accommodative Iol and Monofocal Iol

Shaare Zedek Medical Center

Status: Withdrawn

Conditions: CATARACT SURGERY

Treatments: Device: Acrysof; Device: Acuity's AIOL

Study type: Interventional

Funder types: Other

Identifiers

NCT00604305

6666476CTIL

Rozenman-CWPMS001

Details and patient eligibility

About

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

Full 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.

Sex: All

Ages: 30 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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0 participants in 2 patient groups

Acrysof

Active Comparator group

Description:

Routine monofocal IOL

Treatment:

Device: Acrysof

Acuity's AIOL

Active Comparator group

Description:

Accomodaing IOL

Treatment:

Device: Acuity's AIOL