Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Ophtec USA
Not desired
Age
22–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Patients 22 years of age and over at baseline visit of either sex and of any race where the natural lens has been removed or will be removed and a posterior chamber IOL is not indicated.
Patient must agree to comply with the visit schedule and other requirements of the study
You may not be if
Patients that are not able to meet the extensive postoperative evaluation requirements
Mentally retarded patients
When the patient has no useful vision or vision potential in the fellow eye
History of corneal disease (e.g., herpes simplex, herpes zoster keratitis, etc.), corneal dystrophy, degeneration, opacities or abnormalities that may affect vision.
Abnormality of the iris or ocular structure which would preclude fixation, such as aniridia, hemiiridectomy, severe iris atrophy, rubeosis iridis, or other compromising iris pathology
Patients with uncontrolled glaucoma
High preoperative intraocular pressure, \>25 mmHg
Chronic or recurrent uveitis or history of the same
Preexisting macular pathology that may complicate the ability to assess the benefit or lack of benefit obtained by the lens
Patients with a retinal detachment or a family history of retinal detachment
Retinal disease that may limit the visual potential of the eye such as retinopathy of prematurity or Stargardt's retinopathy Optic nerve disease that may limit the visual potential of the eye
Diabetes mellitus
Pregnant, lactating, or plans to become pregnant during the course of this study
