Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Sensimed AG
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Diagnosis of primary angle closure (PAC) or primary angle closure glaucoma (PACG) with indication for laser peripheral iridotomy (PAC is defined by the presence of a partial or complete iridotrabecular contact in more than 2 quadrants with either raised intraocular pressure \[i.e. more than 21 mmHg\] and/or primary adhesion to the trabecular meshwork (peripheral anterior synechiae \[PAS\]; however, with normal optic disc and visual field. PACG is defined by the presence of iridotrabecular contact with either raised intraocular pressure and/or PAS, and evidence of glaucomatous optic disc and visual field)
No intraocular pressure-lowering drug treatment or a 4-week wash-out period prior to study day 0 and throughout the study
Aged ≥18 years, of either sex
Not more than 6 diopters spherical equivalent on the study eye
Not more than 2 diopters cylinder equivalent on the study eye
Have given written informed consent, prior to any investigational procedure
You may not be if
History of acute angle closure glaucoma
Secondary angle closure glaucoma
History of ocular surgery within the last 3 months
History of ocular laser treatment, including previous laser peripheral iridotomy
Corneal or conjunctival abnormality precluding contact lens adaptation
Severe dry eye syndrome
Patients with allergy to corneal anesthetic
Patients with contraindications for silicone contact lens wear
Patients not able to understand the character and individual consequences of the investigation
Participation in other clinical research within the last 4 weeks
Clareo Health | An Open Label Study Assessing the 24-hour Intraocular Pressure Pattern in PAC and PACG Patients, Before and After Laser Peripheral Iridotomy
