Quality of Vision with the Acrysof Natural Intraocular Lens

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN93782578

Enrollment

Registered

2004-09-30

Start date

2003-12-10

Completion date

Unknown

Last updated

2015-01-13

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

Conditions

Surgery: Cataract Surgery Cataract

Interventions

Randomised, prospective single centre surgical study to determine whether the new Acrysof Natural Intraocular Lens has any significant effect on visual outcome or colour vision post cataract surgery

Eligibility

Inclusion criteria

Inclusion criteria: 20 patients and 20 controls having standard cataract surgery

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Secondary

Measure	Time frame
Not provided at time of registration	—

Primary

Measure	Time frame
1. Colour vision 2. Visual acuity 3. Contrast sensitivity	—

Countries

United Kingdom

Outcome results

None listed

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