24-hour IOP Fluctuation Profile Recorded With SENSIMED Triggerfish in Primary Open-angle Glaucoma (POAG) Patients After Cataract Surgery

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01495299

Enrollment

Registered

2011-12-20

Start date

2011-12-31

Completion date

2012-10-31

Last updated

2019-08-21

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

Conditions

Glaucoma

Keywords

relationship, IOP fluctuations, glaucoma, cataract surgery, SENSIMED Triggerfish

Brief summary

The purpose of this study is to determine the relationship between intraocular pressure (IOP) fluctuations of glaucoma patients as recorded with an IOP-sensing contact lens (SENSIMED Triggerfish®), during two 24-hour periods, before and after cataract surgery. This device has previously been investigated and shown to be safe and well tolerated.

Interventions

DEVICEPhacoemulsification with implantation of intraocular lens (CE-IOL) SENSIMED Triggerfish

Phacoemulsification (standard cataract extraction surgery)

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

Healthy volunteers

Inclusion criteria

* Subject is able to comply with the study procedures * 18-80 years old * Subjects diagnosed with glaucoma, based on presence of repeatable visual field loss and/or glaucomatous optic neuropathy based on masked review of optic disc stereophotographs and under ocular hypotensive treatment, or diagnosed with ocular hypertension, with an IOP of \> 22 mmHg at the screening visit and under ocular hypotensive treatment. * Subject has consented to be in the trial * Visual acuity of 20/200 or better * Presence of cataract requiring phacoemulsification with lens exchange * Ability to understand the character and individual consequences of the study * For women of childbearing potential, adequate contraception

Exclusion criteria

* Subjects presenting with any of the following criteria will not be included in the trial: * Subjects with contraindications for wearing contact lenses * Severe dry eye syndrome * Keratoconus or other corneal abnormality * Conjunctival or intraocular inflammation * Eye surgery prior to and throughout the study. * Full frame metal glasses during SENSIMED Triggerfish® monitoring * Known hypersensitivity to silicone, plaster or ocular anesthesia (proparacaine) * Pregnancy and lactation * Simultaneous participation in other clinical studies

Design outcomes

Primary

Measure	Time frame
24-h IOP patterns	24 hour

Countries

United States

Outcome results

None listed

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