The purpose is to describe the level of visual maturation of premature newborns at term
The secondary purpose is to determine factors associated to an altered level of visual
maturation, through an exploratory approach.
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Full eligibility criteria for NCT02890251
Ages eligible for Study
6 Weeks to 10 Weeks
Genders eligible for Study
Accepts Healthy Volunteers
Infants born before 33 weeks of amenorrhea and hospitalized at CHRU Nancy
All locations for NCT02890251
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Tris trial is registered with FDA with number: NCT02890251. The sponsor of the trial is Central Hospital, Nancy, France and it is looking for 69 volunteers for the current phase.
Official trial title: Visual Maturation in Premature Newborns According to Factors Influencing Its Development
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