24-hr Intraocular Pressure (IOP) Patterns of Glaucoma Patients After Selective Laser Trabeculoplasty (SLT)

Withdrawn before enrolling · Not applicable

Conditions studied: Glaucoma

In brief

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 after selective laser trabeculoplasty (SLT) for routine treatment of glaucoma.

Key facts

Study ID

NCT01495312

Run by

University of California, San Diego

People needed

0

Starts

2011-12-01

Expected to finish

2013-08-12

Last updated by the study team

2019-05-30

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects must correspond to all other inclusion criteria in order to be eligible for the investigation.
• 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
• Ability to understand the character and individual consequences of the study
• For women of childbearing potential, adequate contraception

You may not qualify if…

• 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

Where it is running

• UCSD — La Jolla, California, United States
• UCSD — La Jolla, California, United States

Full record on ClinicalTrials.gov

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