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24h Continuous Intraocular Pressure (IOP) Monitoring vs Goldmann Applanation Tonometry

Comparison of 24-hour Continuous IOP Monitoring With a Contact Lens-based Sensor to Goldmann Applanation Tonometry

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01217853
Enrollment
30
Registered
2010-10-08
Start date
2010-08-31
Completion date
2011-08-31
Last updated
2011-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Open Angle Glaucoma

Brief summary

A study in which intraocular pressure (IOP) will be monitored over 24 hours using the SENSIMED Triggerfish® device and Goldmann applanation tonometry (GAT) in primary open angle glaucoma patients. The aim of this study is to investigate the comparability of diurnal IOP patterns emerging from SENSIMED Triggerfish and GAT.

Interventions

Contact lens-based device for continuous intraocular pressure monitoring

Sponsors

Schlossparkklinik
CollaboratorUNKNOWN
Sensimed AG
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Signed informed consent for the investigation * Patients with primary open angle glaucoma (POAG), defined as open angle ≥ 30°, confirmed visual field loss (Mean Defect/Least Variance ≤ 2dB) and/or optic nerve head damage (cup disc ratio \> 0,5) * Age 40-70 years at inclusion * Not more than 4 diopters spherical equivalent on the study eye * Not more than 2 diopters cylinder equivalent on the study eye * For women of childbearing potential, adequate contraception * Stable anti-glaucomatous therapy 4 weeks before the first 24-hour IOP assessment session and throughout the investigation

Exclusion criteria

* Patients not able to understand the character and individual consequences of the investigation * Patients committed to an institution by virtue of an order issued either by the courts or by an authority * Absence of or withdrawn informed consent * Patients with contraindications for silicone contact lens wear * Wear of full frame metallic glasses during SENSIMED Triggerfish monitoring * Eye disorders including severe dry eye * Eye disorders secondary to POAG * Patient who have had ocular surgery within the last 3 months * Corneal or conjunctival abnormality or irregularity hindering correct contact lens adaptation * Pregnancy and lactation * Allergy to oxybuprocaine (ocular anesthesia) * Simultaneous participation in other clinical research

Design outcomes

Primary

MeasureTime frameDescription
SENSIMED Triggerfish output valuesDuring 24 hoursPatients will undergo one session of 24-hour SENSIMED Triggerfish continuous intraocular pressure monitoring in one eye.
Goldmann applanation tonometry valuesDuring 24 hoursGoldmann applanation IOP readings will be done in the other eye at regular intervals during 24-hour SENSIMED Triggerfish IOP monitoring and in both eyes during another 24-hour session.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026