An observational study in Glaucoma, Ocular Hypertension and Normal Tension Glaucoma, sponsored by Intuor Technologies, Inc.. Completed at 2 sites in United States. Open to participants aged 22 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-11-05.
Sponsored by Intuor Technologies, Inc. · Observational
The CATS Tonometer prism clinical study is intended to determine repeatability of intraocular pressure measurement in human corneas which have undergone a LASIK procedure when compared to a standard Goldmann prism, validating the human LASIK eye findings comparing CATS Tonometer and Goldmann prisms to intracameral pressure in cadaver eyes.
65 studies on the registry are indexed under Low Tension Glaucoma; 10 are open to participants now.
This study's enrollment of 198 is above the median of 94 across 32 observational studies indexed under Low Tension Glaucoma.
Browse Low Tension Glaucoma studies →Intuor Technologies, Inc. is the lead sponsor of 7 studies on the registry; none are open to participants now.
Compared within Low Tension Glaucoma, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Glaucoma. The counts are of registry records indexed under each term, refreshed daily. How we classify →
Subjects must meet the following inclusion criteria to be eligible to participate in this clinical trial:
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Subjects must meet the following inclusion criteria to be eligible to participate in this clinical trial:
Exclusion Criteria:
Subjects will be excluded from participation if they meet the following criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Device: This is observational IOP measurement
Device: This is observational IOP measurement
IOP measurement of patients having LASIK with both CATS and GAT
IOP measurement difference between CATS and GAT in LASIK patients
IOP measurement
Time frame: single measurement 1 day
Plan to share: Undecided — likely will provide deindentified data
No publications or documents are linked to this record.
This study is completed, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.
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Intuor Technologies, Inc.