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Sudden Unexplained Death in Childhood (SUDC) Registry

The SUDC Registry and Research Collaborative

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03109197
Acronym
SUDC
Enrollment
1600
Registered
2017-04-12
Start date
2014-10-01
Completion date
2028-11-30
Last updated
2026-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sudden Unexplained Death in Childhood, Sudden Unexplained Death Syndrome

Brief summary

The purpose is to increase the understanding of the characteristics, circumstances, medical histories and pathologies of children from ages 11 months through 18 years who have died suddenly and unexpectedly, and in some instances, without explanation. The SUDC Registry and Research Collaborative will analyze cases of sudden unexpected deaths in these children to understand risk factors and causes, and develop preventative measures.

Detailed description

* Review the child's death, medical and family history by our study pathologists (including forensic, pediatric, cardiac and neuropathologists) to determine whether a possible, probable or definite cause of death can be identified and whether additional studies might be helpful in determining a specific cause of death. * For case investigations that are open/active, the registry offers cardiac pathology, and neuroimaging/neuropathology consultations. * For those cases determined to be unexplained/undetermined- access to genetic analysis (whole exome sequencing) when viable samples are available. Additional genetic analysis opportunities for biological parents and some family members. For more information, please see our Genetics Frequently Asked Questions. * Study the risks that lead to sudden unexplained death in childhood (SUDC). * Provide families with a review of their child's death through a case review report. * Identify at-risk individuals with the hopes of gaining knowledge to establish prevention strategies to reduce the chances of sudden unexplained death in the future.

Interventions

OTHERBiospecimin Collection

Sponsors

NYU Langone Health
Lead SponsorOTHER
Columbia University
CollaboratorOTHER
Mayo Clinic
CollaboratorOTHER

Study design

Observational model
FAMILY_BASED
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
11 Months to 100 Years
Healthy volunteers
Yes

Inclusion criteria

Retrospective SUDC Cases * 11months to 18 years of age. * Subjects whose cause of death was sudden and unexplained-"Postinfancy SIDS," "Sudden Death of Childhood," "Undetermined," "Late SIDS," a vague description of symptoms of "undetermined etiology," or a diagnosis acknowledged to be speculative by the prosecting pathologist * If the retrospective case has banked DNA specimens. Prospective SUDC Cases * SUDC cases, parents and eligible family members from 11months-100 years of age. * SUDC Subjects whose death was sudden and unexplained after the initial autopsy, and in whom a scene investigation and full autopsy was performed. Family Members Subjects * If the SUDC case has DNA viable specimens, family members will be asked if they would also like to participate in the DNA portion. One or both biological parents if willing and able will be considered as a family subject. * Biological siblings and second degree relatives from age of 0-100 years of age that have had a history or currently have a heart condition and/or neurology condition.

Exclusion criteria

SUDC Subjects * Subjects that are younger than 11months or older than 18 years of age will be excluded as a SUDC case. * Prospective SUDC cases of apparent suicide, homicide, and accident where the external cause was the obvious and only reason for the death will be excluded from this study. Family Member Subjects Any siblings or second degree family relatives that did not have a history or current heart or neurology condition will not be able to enroll in the study.

Design outcomes

Primary

MeasureTime frame
Risks factors leading to sudden unexplained death in childhood (SUDC) collected from PHI5 Years

Countries

United States

Contacts

CONTACTLaura Gould
laura.gould@nyulangone.org
PRINCIPAL_INVESTIGATOROrrin Devinsky, MD

NYU Langone Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 29, 2026