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Visual function, optical disturbance, spectacle independence and patient satisfaction after implantation of trifocal intraocular lens (Acrysof IQ PanOptix) in cataract patients: unilateral versus bilateral implantation.

Visual function, optical disturbance, spectacle independence and patient satisfaction after implantation of trifocal intraocular lens (Acrysof IQ PanOptix) in cataract patients: unilateral versus bilateral implantation.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00029137
Enrollment
80
Registered
2022-07-05
Start date
2020-05-09
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

H26.9

Interventions

Group 1: On patients with cataract a trifocal PanOptix intraocular lens will be bilaterally implanted. A four week distance will be kept between the two operations. Group 2: On patients with cataract

Sponsors

MVZ RHR Augenärzte GmbH Düsseldorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 81 Years

Inclusion criteria

Inclusion criteria: 1. Patients with cataract in both eyes and with a medical indication of a cataract extraction with an implantation of an artificial lens. All the patients have voluntarily and independent from the study decided for a unilateral or bilateral implantation of a trifocal Acrysof IQ PanOptix lens, after a medical enlightenment talk with the treated ophthalmologist. Only capable of consent adults will be included in the study. 2. Age 50-81. 3. No other eye disease. 4. No refractive operation in the patient history. 5. No secondary cataract or already treated secondary cataract with YAG-Laser Kapsulotomy by the time of the evaluation 3 months after the second operation.

Exclusion criteria

Exclusion criteria: 1. Missing patient consent 2. Presence of other eye diseases 3. Postoperative complications that affect the visual aquity 4. Necessity for a re-operation 5. No appearance for the postoperativ evaluation (follow-up).

Design outcomes

Primary

MeasureTime frame
The study´s primary ending point is the patients´visual function and their satisfaction. The primary ending point will be measured three months after the second surgery. By that time the following postoperative measurements will take place (visual acuity, contrast sensitivity, twightlight vision, questionnaire included).

Countries

Germany

Contacts

Public ContactAngelos Simopoulos

MVZ RHR Augenärzte GmbH Düsseldorf,Heinrich Heine Universität Düsseldorf

angelos.simopoulos@gmail.com00491735635780

Outcome results

None listed

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