Clinical Trial

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

Study acronym: PROACTIVE NYS
Recruiting
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Record status
This record was last updated May 13, 2025 (before its estimated October 1, 2025 completion). Its status may not reflect the trial's current state.
Summary
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.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-01-23; most recent amendment 2025-05-12.
Status change: Not Yet Recruiting → Recruiting 2024-04-15
Trial Details
NCT Number NCT06226558
Lead Sponsor Stony Brook University
Collaborators: Frontier Science & Technology Research Foundation, Inc.
Conditions Congenital CMV Infection, Sensorineural Hearing Loss
Enrollment 1,000 participants
Start Date 2024-02-01
Primary Completion 2025-10-01 (estimated)
Study Completion 2026-10-01 (estimated)
Updated on ClinicalTrials.gov 2025-05-13