glaucoma
Conditions
Interventions
Measure diurnal variation of intraocular pressure before and 1-3 months after the addition of glaucoma treatment for patients determined to require additional glaucoma treatment.
Sponsors
Tokai University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Males and females over 20 years of age at the time of registration 2) Patients with glaucoma, preperimetric glaucoma, ocular hypertension, and angle-closure glaucoma who require additional glaucoma treatment 3) Patients who have received sufficient explanation about participation in this research and have obtained written consent of their own free will
Exclusion criteria
Exclusion criteria: 1) Patients who cannot wear contact lenses (patients with contraindicated target diseases as listed in the Triggerfish package insert) 2) Patients who have a history of intraocular surgery within the past 3 months in the test eye 3) Patients who have a history of refractive surgery in the past 4) Patients with a history of glaucoma surgery in the past 5) Patients with keratoconus or other corneal diseases 6) Patients with conjunctivitis or endophthalmitis 7) Other patients who are deemed unsuitable for inclusion in the subject by the physician's judgment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the absolute difference between the highest and lowest contactlens sensor values (mVeq), as measured by the triggerfish before and 1-3 month after the addition of glaucoma treatment. | — |
Countries
Japan
Contacts
Public ContactTakashi Matsushima
Tokai University School of Medicine Department of Ophthalmology
Outcome results
None listed