Trials / Completed
CompletedNCT01972997
SENSIMED Triggerfish Sensor Sizes
A Single-center, Randomized, Double-blinded, Prospective Study to Assess the Changes in the 24-hour IOP (Intraocular Pressure) Pattern in Relation to SENSIMED Triggerfish® Sensor Sizes in Healthy Subjects
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 14 (actual)
- Sponsor
- Sensimed AG · Industry
- Sex
- All
- Age
- 18 Years – 100 Years
- Healthy volunteers
- Accepted
Summary
This is a study investigating the effect of various SENSIMED Triggerfish sensor lens sizes on the recorded IOP related patterns in 10 healthy volunteers. Each volunteers receives 4 24-hours sessions of pattern recording on one selected eye (study eye). Each of the sensor lens sizes is placed on the eye in the different sessions. Subjects visit the study site for installation and removal of the device and accompanying exams, but remain ambulatory during the recording.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | SENSIMED Triggerfish |
Timeline
- Start date
- 2013-07-01
- Primary completion
- 2014-03-01
- Completion
- 2014-03-01
- First posted
- 2013-10-31
- Last updated
- 2015-11-17
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT01972997. Inclusion in this directory is not an endorsement.