Implantation of a new intraocular lens for patients who require a new lens

One year outcomes and stability of a novel scleral anchored intraocular lens

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN10015880

Enrollment

Registered

2021-06-29

Start date

2017-11-01

Completion date

Unknown

Last updated

2022-04-25

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

Conditions

Aphakia Eye Diseases Aphakia

Interventions

The study is a single arm trial. All patients underwent surgery consisting of vitrectomy, removal of dislocated lens and implantation of scleral fixation intraocular lens at baseline. Postoperative fo

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Postoperative or posttraumatic aphakia or late dislocation of IOL and or capsular bag

Exclusion criteria

Exclusion criteria: 1. Corneal opacities 2. Visually significant macular diseases 3. Retinal detachment 4. Optic disk atrophy 5. Advanced glaucoma 6. Any other ocular condition that was likely to compromise the functional outcome

Design outcomes

Primary

Measure	Time frame
Visual acuity was measured in decimal Snellen units and then converted in Logarithm of minimum angle resolution (LogMAR) for statistical purposes assessed at baseline and at 1,3,6 and 12 months follow up	—

Secondary

Measure	Time frame
Assessed at baseline and at 1,3,6 and 12 months follow up 1. IOL stability was assessed comparing the angle, in degrees, between IOL optic and posterior iris plane. 2. Complications assessed using patient records	—

Countries

Italy, San Marino

Outcome results

None listed

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