Last reviewed · How we verify

NCT03480906

Eyenovia MiDD Usability Study

Completed NA Last updated 26 July 2018
What this trial tests

NA trial testing Latanoprost in Intraocular Pressure in 30 participants. Completed in 17 March 2018.

Timeline
12 March 2018
Primary endpoint
17 March 2018
17 March 2018

Quick facts

Lead sponsorEyenovia Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designcrossover
Maskingsingle
Primary purposeother
Enrollment30
Start date12 March 2018
Primary completion17 March 2018
Estimated completion17 March 2018
Sites1 location across Panama

Drugs / interventions tested

Conditions studied

Sponsor

Eyenovia Inc. — full company profile →

Who can join

18 and older, any sex, with Intraocular Pressure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is to evaluate the usability and patient tolerability for microtherapeutic dosing of commercially available ocular medication via the Eyenovia microdose delivery system (MiDD)

Publications & conference data

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

Verify or expand the search:

Other trials of Latanoprost

Trials testing the same drug.

Other recruiting trials for Intraocular Pressure

Currently open trials in the same condition.

Other Eyenovia Inc. trials

Trials by the same sponsor.

Verify against primary sources

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/NCT03480906.

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