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NCT05772780

MP-3 Biofeedback Training and Central Vision Loss

Completed NA Last updated 16 March 2023
What this trial tests

NA trial testing MP-3 microperimeter in Age-Related Macular Degeneration in 24 participants. Completed in 9 February 2022.

Timeline
1 October 2021
Primary endpoint
9 February 2022
9 February 2022

Quick facts

Lead sponsorAmore Filippo
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment24
Start date1 October 2021
Primary completion9 February 2022
Estimated completion9 February 2022
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Amore Filippo

Who can join

Adults 20 to 80, any sex, with Age-Related Macular Degeneration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objectives of this investigation are: * evaluate the results of rehabilitation treatment using photostimulation with a structured stimulus in two different samples of low vision subjects with central vision loss who will be subjected to biofeedback at the MP3 microperimeter with different timing; * compare the effectiveness of the rehabilitation treatments in the two groups to provide useful indications for proposing standardisation of the rehabilitation pathway focusing on photostimulation in subjects with central vision loss.

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 Age-Related Macular Degeneration

Currently open trials in the same condition.

Other Amore Filippo 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/NCT05772780.

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