Central Corneal Thickness With SENSIMED Triggerfish (09/08)

Sensimed

Status: Completed

Conditions: Glaucoma; Ocular Hypertension

Treatments: Device: SENSIMED Triggerfish

Study type: Observational

Funder types: Industry

Identifiers

NCT01210963

09/08

Details and patient eligibility

About

Investigation of the occurrence of possible corneal swelling after continuous Intraocular pressure (IOP) monitoring with a contact lens-based Sensor during the sleeping period.

Enrollment: 20 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• glaucoma and ocular hypertension scheduled for overnight hospitalisation
• stable IOP-lowering treatment since at least 4 weeks before study
• at least 18 years
• having provided informed consent

Exclusion criteria

• contact lens wear within the last 2 years
• contraindication for silicone lean wear
• corneal abnormality in either eye
• ocular infection or inflammation
• history of ocular surgery within the last 3 months
• full-frame metal glasses during IOP monitoring with SENSIMED Triggerfish
• pregnancy and lactation
• patients not able to understand the nature of the research
• patients under tutelage
• patients committed to an institution by virtue of an order issued either by the courts or by an authority
• simultaneous participation in other clinical research

Trial design

20 participants in 1 patient group

SENSIMED Triggerfish

Treatment:

Device: SENSIMED Triggerfish