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Study identifier: NCT06226558 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Long-Term Outcomes of Children With Congenital CMV in New York State

Condition: Congenital CMV Infection · Sensorineural Hearing Loss  ·  Sponsor: Stony Brook University

PhaseN/A
Planned participants1000
Who can joinAll sexes, 0 Days to 1 Year
Healthy volunteersNo

About this study

PROACTIVE NYS is a long-term follow-up study of all infants who test positive for congenital Cytomegalovirus infection (CMV) throughout New York State on the Newborn Screen. By following all infants who screen positive, we will learn important information about the range of symptoms caused by congenital CMV, from those babies with more severe findings to those with no symptoms. In particular, our study will provide new information about many facets of congenital CMV, including: * Developmental, hearing, neurologic, and vision outcomes * The spectrum and timing of symptoms * The impact congenital CMV has on the baby and its family * How many babies are infected with congenital CMV in New York State How antiviral medications and other interventions impact outcomes of children with congenital CMV Throughout the duration of the study, children will undergo routine developmental and hearing assessments, which will assist with early diagnosis of any infection complications. Any child found to have a neurodevelopmental, hearing, or vision abnormality will be referred for appropriate evaluation and treatment. Families will also be asked to complete periodic surveys about their experience with congenital CMV, both as a medical diagnosis and as it affects their day-to-day activities.

This description comes directly from the study's public registry record.

Talk to the study team

Andrew Handel, MD  ·  631-444-7692  ·  Andrew.handel@stonybrookmedicine.edu

Sharon Nachman, MD  ·  631-444-7692  ·  sharon.nachman@stonybrookmedicine.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Stony Brook Children's HospitalStony Brook, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06226558