Use of an Ocular Telemetry Sensor in Diamox Treated Patients
Not Applicable
Completed
- Conditions
- GlaucomaOcular Hypertension
- Interventions
- Device: SENSIMED Triggerfish
- Registration Number
- NCT01028664
- Lead Sponsor
- Sensimed AG
- Brief Summary
A soft contact lens integrating a Sensor is placed on subjects with high intraocular pressure (IOP) after administration of an IOP-lowering drug to investigate the device's capacity to detect the induced IOP reduction.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
- Confirmed diagnosis of glaucoma or ocular hypertension
- IOP of ≥ 15 mmHg.
- Patients of either gender.
- Older than 18 years.
- Patients who accept signing an informed consent approved by the Ethics Committee.
Exclusion Criteria
- Patients not able to understand the nature of the research
- Patients under tutorship
- Corneal abnormalities in both eyes
- Subjects with contraindications for wearing contact lenses
- History of ocular surgery within the last 3 months
- Known hypersensitivity to Diamox® or to any of its excipients
- Pregnancy and lactation
- Simultaneous participation in other clinical research
- Patients with evidence of ocular infection or inflammation
- History of renal or hepatic impairment, hypokalemia and hyponatremia
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Glaucoma or ocular hypertension patients SENSIMED Triggerfish -
- Primary Outcome Measures
Name Time Method Detection of IOP reduction 2 hours after Diamox administration 2 hours
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Clinique de Montchoisi, Centre du Glaucome
🇨🇭Lausanne, Switzerland