Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

Intraocular Pressure Measured by a Novel Sensing Contact Lens Versus Tonometry

NCT: NCT04024293 · RECRUITING

NCT IDNCT04024293
StatusRECRUITING
Start Date2025-10-01
Completion2026-05

Brief Summary

While elevated intraocular pressure (IOP) is no longer part of the definition of glaucoma it remains the sole proven modifiable risk factor for the onset and progression of glaucoma. IOP is known to vary with the time of day as well as with daily activities. The importance of the nycthemeral IOP pattern for successful management of glaucoma has been well documented, especially for patients who experience visual loss despite apparently normal and/or controlled IOP during office hours. The current way of assessing nycthemeral IOP fluctuation is to perform repeated discrete tonometry measurements, once per hour in the best cases. Since its development in the 50s, Goldmann applanation tonometry (GAT) has remained the gold standard method for measuring IOP, despite its limitations. However, tonometry may be an imperfect method for measuring changes in IOP because it allows only snapshot and non-continuous measurements, it is not physiologic and disturbs the sleep architecture. There have been many efforts in the past decades to search for an ambulatory and frequent method to monitor IOP for 24 hours. In this context, Sensimed AG has recently developed a sensing contact lens-based device intended to measure IOP over 24 hours, the Goldfish (GF). First-in-man data obtained with this device showed agreements between IOP measured by GF and values obtained by standard tonometry in the same eye, comparable to literature results for routinely used tonometry devices. However, this pilot study included 9 subjects only with improvable safety, tolerability and efficacy profiles. The main goal of this study is to assess IOP measurements with the GF and compare the values with those obtained by standard tonometry in patients with open angle glaucoma (OAG) and ocular hypertension (OHT).

Frequently Asked Questions

What is Intraocular Pressure Measured by a Novel Sensing Contact Lens Versus Tonometry?

Intraocular Pressure Measured by a Novel Sensing Contact Lens Versus Tonometry is a clinical trial registered under NCT04024293. Current status: RECRUITING.

What is the status of NCT04024293?

The current status of NCT04024293 (Intraocular Pressure Measured by a Novel Sensing Contact Lens Versus Tonometry) is: RECRUITING.

When did Intraocular Pressure Measured by a Novel Sensing Contact Lens Versus Tonometry start?

Intraocular Pressure Measured by a Novel Sensing Contact Lens Versus Tonometry started on 2025-10-01.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.