H40.1
Conditions
Interventions
Group 1: Microshunt+Healaflow
Patients’ spherical equivalents were obtained by the auto refractometer Nidek AR-1s (Oculus GmbH, Wetzlar, Germany). Intraocular pressure was obtained using Goldmann appl
Sponsors
Ludwig Maximilians Universität München
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria include patients with moderate to severe POAG requiring treatment due to inadequate intraocular pressure despite local pressure-lowering therapy or with eye drop intolerance with or without previous (MIGS) surgery. Exclusion criteria include combined procedure with cataract surgery, silicone oil tamponade, partner eye already included in the study, age younger than 18, selective laser trabeculoplasty within the last 90 days preoperatively.
Exclusion criteria
Exclusion criteria: Exclusion criteria include combined procedure with cataract surgery, silicone oil tamponade, partner eye already included in the study, age younger than 18, selective laser trabeculoplasty within the last 90 days preoperatively.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intraocular presssure Intraocular pressure was measured using a Goldmann applanation tonometer. Measurements were taken two days, 1–2 weeks, 4–6 weeks, 3–4 months, and 5–6 months after surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Medication The number of intraocular pressure-lowering eye drops was asked during each visit. The visits took place two days, 1–2 weeks, 4–6 weeks, 3–4 and 5–6 months after the operation. | — |
Countries
Germany
Contacts
Public ContactLeonie Keidel
Ludwig Maximilians Universität München
Outcome results
None listed