Effect of a plate haptic design on intraocular lens rotational-and-axial stability and posterior capsule opacification: a randomised trial (acrismart versus acrilyc intraocular lenses)

Effect of a plate haptic design on IntraOcular Lens rotational-and-axial stability and posterior capsule opacification: a randomised trial (Acrismart versus Acrilyc IntraOcular Lenses)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN01285948

Enrollment

Registered

2007-01-29

Start date

2006-11-28

Completion date

Unknown

Last updated

2016-10-17

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

Conditions

Cataract

Interventions

Intraocular lens implant (Acrismart or Acrylic lens)

Eligibility

Inclusion criteria

Inclusion criteria: 1. Bilateral age-related cataract 2. Age 40 and older 3. Visual Acuity more than 0.05 4. Written informed consent to surgery and participation in the study

Exclusion criteria

Exclusion criteria: Relevant other ophthalmic diseases (such as pseudoexfoliation, glaucoma, traumatic cataract and other comorbidity that could affect Posterior Capsule Opacification (PCO) rate, axial and rotational stability (e.g. Marfan syndrome)

Design outcomes

Primary

Measure	Time frame
Posterior capsule opacification (%)	—

Secondary

Measure	Time frame
1. Orientation (degrees) 2. Anterior Chamber Depth (ACD) (mm) 3. Decentration (mm) 4. Refraction 5. Rhexis size (mm^2) 6. Slitlamp biomicroscopy (descriptive)	—

Countries

Austria, United Kingdom

Outcome results

None listed

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