H25-H28
Conditions
Interventions
Group 1: Implantation of one new intraocular lens into minimum of one eye. The other eye may receive a standard IOL if there is no existing corneal astigmatism.
Sponsors
AMO Germany GmbH
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Healthy patients with bilateral cataracts; women shall not be pregnant or breast-feeding
Exclusion criteria
Exclusion criteria: Uncontrolled systemic or ocular deseases; participating in another study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The placement of the intraocular lens will be determined 1 day postoperatively and compared with the 3-months postoperative data. The visual acuity for far and near will be evaluated quantitively the 1-week postoperative examination onwards. | — |
Secondary
| Measure | Time frame |
|---|---|
| Side effects/complications will be evaluated at each postoeprative examination. Patient satisfaction will be evaluated preoperatively and at the final postoperative examination. | — |
Countries
Austria, Germany, Spain
Contacts
Public ContactRoland Pohl
AMO Germany GmbH
Outcome results
None listed