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NCT05675917: MACUTEST

MacuTest Website for Personalized AMD Risk Prediction and Prevention

Withdrawn NA Last updated 12 February 2024
What this trial tests

NA trial testing MacuTest platform in Macular Degeneration. Withdrawn.

Timeline
2 February 2024
Primary endpoint
2 February 2024
2 February 2024

Quick facts

Lead sponsorUniversity Hospital, Bordeaux
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Start date2 February 2024
Primary completion2 February 2024
Estimated completion2 February 2024

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Bordeaux

Who can join

65 and older, any sex, with Macular Degeneration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

LEHA team of Bordeaux University has developed an Age-related Macular Degeneration (AMD) prediction algorithm (taking into account age, 49 genetic variants, the presence of early retinal abnormalities, tobacco consumption, food quality, blood pressure and education level) and is currently developing the MacuTest website, integrating this prediction algorithm. This platform offers participants the possibility to enter their personal lifestyle data, to couple them with an ophthalmological examination and a genetic test, in order to evaluate their personalized risk of AMD. The main objective of this pilot study is to evaluate the feasibility of estimating the predicted AMD risk

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Macular Degeneration

Currently open trials in the same condition.

Other University Hospital, Bordeaux 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/NCT05675917.

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