Table 1.
Gonio scratch study synopsis
| Purpose | To compare the efficacy and safety of gonio scratch surgery | |
| Patient eligibility | ||
| Inclusion criteria | ≥20 years of age | |
| Patients who are scheduled to undergo glaucoma surgery | ||
| Patients who can complete outpatient visits within 1 year after the surgery | ||
| Written informed consent | ||
| Exclusion criteria | Pregnant or nursing women | |
| Patients who underwent an intraocular surgery within the previous 6 months | ||
| Patients who cannot measure intraocular pressure with a Goldmann applanation tonometer | ||
| Neovascular glaucoma patients | ||
| Patients with an intraorbital tumor behind the eye, thyroid eye disease, Sturge–Weber syndrome, or other diseases that increase superior scleral venous pressure | ||
| Patients who are allergic to nitinol | ||
| Patients recognized by the physician as inappropriate for this study | ||
| Follow-up examination | 1 day, 1 week, 1 month, 3 months, 6 months, and 1 year after surgery | |
| Outcome measures | Intraocular pressure | |
| Surgical time | ||
| Number of glaucoma medications | ||
| Visual acuity | ||
| Visual fields | ||
| Enrollment | 80 eyes | |
| Study centers and committees | Four clinical eye centers: | |
| Hiroshima University Hospital | ||
| Miyoshi Eye Clinic | ||
| Yokoyama Retina Clinic | ||
| Kusatsu Eye Clinic | ||