H33.0 H25.9 H40.1 H18.5 H18.6 H04.5 H27.0 H35.3 H40.5 H17.9
Conditions
Interventions
Group 1: New, minimally invasive ophthalmic surgical procedures
Group 2: Conventional ophthalmic surgical procedures
Sponsors
Uniklinik RWTH Aachen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Indication for the corresponding eye surgery 2. Age of majority 3. Written declaration of consent to the ADDA study 4. Persons who are legally competent and mentally capable to accomplish the instructions of the examiner
Exclusion criteria
Exclusion criteria: 1. Pregnant and nursing women 2. Individuals living in an institution due to official or judicial instruction 3. Individuals who are dependent or have an employment relationship with the examiner
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Success rates at 1 month, 3 months, 6 months, 12 months, 24 months, 36 months follow-up. Definition of primary endpoints depends on the performed surgery. For example: - Lens surgery: successful artificial lens implantation and visual acuity improvement - Keratoplasty: successful implantation of the corneal graft and visual acuity improvement - Glaucoma surgery: lowering the intraocular pressure - Retinal surgery: retinal detachment: reattachment of the retina / Macular hole: closure / Gliosis: recovery of macular morphology - Lacrimal surgery: creation of a functional pathway from the canaliculi into the nose - further | — |
Secondary
| Measure | Time frame |
|---|---|
| -Complication rates -Further relevant eye parameters, e.g. visual acuity, intraocular pressure, perimetry, refraction, keratometry, anatomical OCT parameters, quality of life | — |
Countries
Germany
Contacts
Public ContactMatthias Fuest
Uniklinik RWTH Aachen
Outcome results
None listed