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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05865093
Other study ID # 5006
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2022
Est. completion date June 30, 2027

Study information

Verified date May 2023
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact Daniela Ricci, Medical Doctor
Phone +393929477842
Email d.ricci@iapb.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to assess visual function from neonatal age to 36 months of age in infants at risk of visual impairment due to brain lesion or ocular pathology


Recruitment information / eligibility

Status Recruiting
Enrollment 700
Est. completion date June 30, 2027
Est. primary completion date September 30, 2023
Accepts healthy volunteers No
Gender All
Age group 2 Days to 36 Months
Eligibility Inclusion Criteria: - Age between 34 weeks of post-menstrual age and 36 months of life in children born before 37 weeks gestational age - Genetic syndroms - Hypoxic Hischemic Encephalopathy - Brain malformation - Metabolic diseases - Ocular pathologies Exclusion Criteria: - Patients at low risk of developing neurological outcomes - Refusal of informed consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy Fondazione Policlinico Gemelli Rome

Sponsors (1)

Lead Sponsor Collaborator
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Early Visual Functions in Patients at Risk of Developing Cerebral Visual Impairment. A Pilot Study The score of the functional visual assessment will be obtained at neonatal age and at 1-3-6-9-12-18-24-36 months of life will be analysed at each age and compared to neurodevelopment findings using different scales according to age.
These results will be related to the MRI total score (obtained by the sum of scores by site: cortex, basal ganglia, white matter and cerebellum, normal (0), mild abnormal (1), severely abnormal (2)).
5 years
Secondary Correlation betwwen functional visual assessment score to MRI score Results of functional visual assessment will be related to the MRI total score (obtained by the sum of scores by site: cortex, basal ganglia, white matter and cerebellum, normal (0), mild abnormal (1), severely abnormal (2)). 5 years
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