Actively Recruiting

All Genders
Healthy Volunteers
NCT01662453

Risk Factors for Sudden Unexplained Death in Epilepsy

Led by NYU Langone Health · Updated on 2025-07-30

800

Participants Needed

1

Research Sites

795 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main purpose of this study is to develop a North American registry for SUDEP cases; requesting family members of epilepsy patients who died suddenly of unclear causes (SUDEP) to contact the study team. The family members who decide to participate in the study will be asked to complete a brief telephone interview about their loved one's epilepsy and seizure history and the circumstances of his or her death. If the death has occurred within the past 24 hours, and the family is willing to consider donating tissue to the study, the subject will be transferred to the Autism Tissue Program, and the remainder of the phone interview will be conducted at a later time. In addition to the phone interview, the family will be asked to provide access to the deceased's medical records. Any costs involved in obtaining medical records will be covered by the study, and all medical information will remain completely confidential.

CONDITIONS

Official Title

Risk Factors for Sudden Unexplained Death in Epilepsy

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects diagnosed with epilepsy whose cause of death was sudden and unexplained, with families willing to participate
  • Patients diagnosed with epilepsy currently under the care of the NYU Comprehensive Epilepsy Center who are willing and able to participate
Not Eligible

You will not qualify if you...

  • Not explicitly provided in the source

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

NYU Comprehensive Epilepsy Center

New York, New York, United States, 10016

Actively Recruiting

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Research Team

J

Juliana Laze

CONTACT

M

Marlene Cosme

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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