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NCT05416268

Study to Compare the Diopsys NOVA and LKC RETeval Devices

Completed NA Last updated 14 June 2022
What this trial tests

NA trial testing Electroretinography in Retinal Disease in 20 participants. Completed in 6 May 2022.

Timeline
4 May 2022
Primary endpoint
6 May 2022
6 May 2022

Quick facts

Lead sponsorDiopsys, Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designcrossover
Maskingnone
Primary purposediagnostic
Enrollment20
Start date4 May 2022
Primary completion6 May 2022
Estimated completion6 May 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Diopsys, Inc.

Who can join

22 and older, any sex, with Retinal Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To compare the Diopsys NOVA and LKC RETeval Devices using the Diopsys Lid Electrodes and LKC RETeval Self-Adhering Electrode Arrays.

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 recruiting trials for Retinal Disease

Currently open trials in the same condition.

Other Diopsys, 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/NCT05416268.

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