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NCT03207477: PrmvsionSuiv

Premavision Cohort Follow-up

Terminated NA Last updated 13 August 2021
What this trial tests

NA trial testing Visual acuity measurement in Visual Disorder in 37 participants. Terminated before completion.

Timeline
20 November 2017
Primary endpoint
30 June 2020
30 June 2021

Quick facts

Lead sponsorCentral Hospital, Nancy, France
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposescreening
Enrollment37
Start date20 November 2017
Primary completion30 June 2020
Estimated completion30 June 2021
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Central Hospital, Nancy, France

Who can join

Adults 18 Months to 7, any sex, with Visual Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aim at following a cohort of prematurely born infants at 18 months corrected age, 4 and 7 years of age. This cohort had an evaluation of visual maturation at term equivalent age (TEA) with factors associated with impaired visual maturation. (PREMAVISION-CLinicalTrials.gov ID: NCT02890251). In this follow-up study, prematurely born infants vision will be compared to term born infants matched for postnatal age.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Visual acuity measurement

Trials testing the same drug.

Other Central Hospital, Nancy, France trials

Trials by the same sponsor.

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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/NCT03207477.

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