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

NCT06607705 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 53

Last updated 2025-03-06

No results posted yet for this study

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.

Conditions

  • Glaucoma Eye

Interventions

DEVICE

Monitoring with contact lens sensor

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

DEVICE

Monitoring with contact lens sensor

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

DEVICE

Monitoring with contact lens sensor

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

Sponsors & Collaborators

  • Glaukos Corporation

    collaborator INDUSTRY

  • Fundacio Privada Mon Clinic Barcelona

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-21
Primary Completion
2025-10-01
Completion
2025-10-01

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06607705 on ClinicalTrials.gov