Sleep Apnea Syndrome
Conditions
Interventions
The enrollees were admitted overnight for continuous IOP monitoring using the SENSIMED Triggerfish CLS (Sensimed AG, Lausanne, Switzerland). They underwent Sandman Elite polysomnograpy (Version 7.2, E
Sponsors
Hokkaido University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Patient age of 20 years or older at the time of obtaining informed consent 2.Glaucoma patients with SAS was suspected in the interview, or SAS patients without galucoma 3.Patients after receiving a sufficient explanation upon participation in this study, on the thorough understanding, that document consent is obtained by the free will of the patient himself.
Exclusion criteria
Exclusion criteria: 1.Patients to merge the disease that produces a field of view failure in addition to glaucoma 2.Patients wearing contact lenses is not possible in severe dry eye 3.Some of the history of complications or infection of the eye associated with contact lens wear 4.Patients with active infection in their eyes 5.Patients with ocular trauma 6.Patients who recently underwent eye surgery 7.Patients with a history of silicon allergy 8.Patients with hypersensitivity to the tape and seal 9.Patients with a history of dry eye
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Continuous IOP measurement | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart rate Respiratory rate Oxygen saturation | — |
Countries
Japan
Contacts
Public ContactRiki Kijima
Hokkaido University Graduate School of Medicine Department of Ophthalmology
Outcome results
None listed