RecruitingNot ApplicableNCT06607705

Changes in Eye Pressure in Glaucoma Patients Treated with Istent Inject W, Monitored by a Contact Lens Sensor

Fluctuations of the Intraocular Pressure in Surgically Treated Glaucoma Patients with IStent Inject W by a Contact Lens Sensor


Sponsor

Fundacio Privada Mon Clinic Barcelona

Enrollment

53 participants

Start Date

Oct 21, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to compare the IOP-related fluctuations using the CLS (contact lens sensor) Sensimed Triggerfish in glaucoma patients before and after glaucoma surgery with iStent inject W under physiological conditions and compare these results with a control group of glaucoma patients treated only with hypotensive medical treatment requiring cataract surgery.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study monitors eye pressure changes around the clock in glaucoma patients who have received a tiny implant called iStent inject W, which helps drain fluid from the eye to lower pressure. Participants wear a special contact lens sensor that continuously tracks eye pressure to give doctors a more complete picture than occasional office measurements. **You may be eligible if...** - You are 18 years or older - You have been diagnosed with primary open-angle glaucoma (POAG), normal tension glaucoma (NTG), or ocular hypertension (elevated eye pressure without glaucoma damage) - You have received the iStent inject W implant as part of your treatment - Your untreated eye pressure was above 21 mmHg at diagnosis **You may NOT be eligible if...** - You have conditions that caused your elevated eye pressure (e.g., narrow angles, blood vessel growth on the iris, inflammation) - You cannot tolerate the contact lens sensor - You do not meet the diagnostic criteria for POAG, NTG, or ocular hypertension Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEMonitoring with contact lens sensor

Monitoring with contact lens sensor at 1-month pre-intervention visit

DEVICEMonitoring with contact lens sensor

Monitoring with contact lens sensor at 1-month post-intervention visit

DEVICEMonitoring with contact lens sensor

Monitoring with contact lens sensor at 3-months post-intervention visit


Locations(2)

Institut Català de Retina

Barcelona, Spain, Spain

Hospital Clínic de Barcelona

Barcelona, Spain, Spain

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NCT06607705


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