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NCT06186388

Glaucoma Screening

Completed NA Last updated 26 August 2024
What this trial tests

NA trial testing TEMPO iMOvifa in Glaucoma in 200 participants. Completed in 15 May 2024.

Timeline
5 December 2023
Primary endpoint
15 May 2024
15 May 2024

Quick facts

Lead sponsorCape Fear Eye Institute
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment200
Start date5 December 2023
Primary completion15 May 2024
Estimated completion15 May 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Cape Fear Eye Institute

Who can join

40 and older, any sex, with Glaucoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

* The primary objective of this study is to evaluate the diagnostic accuracy of the TEMPO (iMOvifa) visual field perimeter screening test by measuring the sensitivity in a population of eyes with glaucoma and the specificity in a population of normal eyes and to measure repeatability of the screening test. * The secondary objective of this study is to gather and analyze ancillary data to confirm the diagnosis or absence of glaucoma.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Glaucoma

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06186388.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing