NCT02981186

Comparison of Visual Outcomes After Implantation of the POD AY GF F (PhysIOL) and the POD AY 26P F (PhysIOL)

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 25 (actual)
• Sponsor: Beaver-Visitec International, Inc. · Industry
• Sex: All
• Age: 50 Years
• Healthy volunteers: Accepted

Summary

The study is a prospective randomised controlled study. The patients get monolateral IOL implantation of POD F GF and POD F in the contralateral eye. Both IOLs are trifocal IOLs consisting of the same optical design. The difference between the IOLs is the material (hydrophilic and hydrophobic). To decide which eye receives POD F and which eye receives POD F GF, a randomization table will be provided to the principle investigator.

Detailed description

The examinations consist of visual acuity data, contrast sensitivity exams and slitlamp examinations. Follow up will be up to 6 months postoperative.

Conditions

• Cataract
• Lens Opacity

Interventions

Type	Name	Description
DEVICE	IOL implantation experimental	Implantation of trifocal IOL POD F GF consisting of hydrophobic material
DEVICE	IOL implantation comparator	Implantation of trifocal IOL POD F consisting of hydrophilic material

Timeline

• Start date: 2016-11-02
• Primary completion: 2017-09-25
• Completion: 2017-09-25
• First posted: 2016-12-05
• Last updated: 2021-05-06

Locations

1 site across 1 country: Hungary