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Status unknownNCT03074279PRERIESUpdated Mar 8, 2017

Risk Factors of SUDEP

An observational study in Epilepsy, sponsored by University Hospital, Montpellier. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-03-08.

Sponsored by University Hospital, Montpellier · Observational

The sponsor has not verified this record recently (last verified Mar 2017), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
408
Ages
18 Years and older
Sex
All
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Study summary

Numerous studies over the past decade have shown without any doubt that there is a higher mortality risk in patients with epilepsy than in the general population. The cause of death may be related to the cause of epilepsy, being directly related to a seizure (status epilepticus or sudden unexpected death in epilepsy; SUDEP), a consequence of seizures (accidents, etc), other associated pathologies (cancer, cardiovascular disease, ischemic heart disease, pneumonia, etc) or an associated disorder (depression or suicide). A SUDEP is defined as a sudden, non-traumatic, unexpected death in a patient with epilepsy, not necessarily in the presence of witnesses, that is not due to drowning, with or without evidence of a seizure, excluding documented status epilepticus and in which a post-mortem autopsy reveals no anatomical or toxicological cause of death. Little is known about SUDEP and its mechanisms and risk factors.

This epidemiological study is based on the RSME. The Main objective of this study to identify risk factors of SUDEP, in particular night-time supervision and the risks associated with anti-epileptic drugs including compliance and drug interactions.

Read the detailed description

Numerous studies over the past decade have shown without any doubt that there is a higher mortality risk in patients with epilepsy than in the general population. The cause of death may be related to the cause of epilepsy, being directly related to a seizure (status epilepticus or sudden unexpected death in epilepsy; SUDEP), a consequence of seizures (accidents, etc), other associated pathologies (cancer, cardiovascular disease, ischemic heart disease, pneumonia, etc) or an associated disorder (depression or suicide). A SUDEP is defined as a sudden, non-traumatic, unexpected death in a patient with epilepsy, not necessarily in the presence of witnesses, that is not due to drowning, with or without evidence of a seizure, excluding documented status epilepticus and in which a post-mortem autopsy reveals no anatomical or toxicological cause of death. Little is known about SUDEP and its mechanisms and risk factors.

A French national network on epilepsy related death (Reseau Sentinelle Mortalité Epilepsie, RSME) will be initially established in 2010 by the French League Against Epilepsy (LFCE) under the leadership of bereaved families and supported by the French Foundation for Epilepsy Research (FFRE). This epidemiological study is based on the RSME.

The Main objective of this study to identify risk factors of SUDEP, in particular night-time supervision and the risks associated with anti-epileptic drugs including compliance and drug interactions.

The study design is an epidemiological case-control study. The cases are SUDEP identified in the RSME and French centres of Epileptology.

Epilepsy-related deaths are reported by physicians but also by bereaved families. An interview with a psychologist will be proposed at this moment.

The control group will include patients with epilepsy and relatives of patients from tertiary epilepsy units (in particular, participants of GRENAT registry or a national multicenter study RESPOMSE), private neurologists or general practitioners and thanks from patients associations.

Sociodemographic data, lifestyle, personal and family medical history will be collected during an interview with a psychologist by phone or during a face to face interview. For bereaved families, information on causes and circumstances of beloved one's death will be collected during these interviews.The characteristics of epilepsy will be completed by the patient's neurologist.

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Conditions studied

  • Epilepsy

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Keywords

  • Epilepsy
  • SUDEP
  • case-control study
  • risks factors
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In context

Epilepsy

1,805 studies on the registry are indexed under Epilepsy; 417 are open to participants now.

This study's planned enrollment of 408 is above the median of 102 across 521 observational studies indexed under Epilepsy.

Browse Epilepsy studies →

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Cases : Confirmed or probable SUDEP or nearSUDEP reported by physicians of the "Réseau Sentinelle Mortalité Epilepsie" (RSME) or by bereaved families. The bereaved families will be contacted by a psychologist who proposes an interview.

Controls : Patients with epilepsy and relatives of patients recruited from tertiary epilepsy units, private neurologists or general practitioners and thanks from patients associations.

Inclusion criteria

Cases : Any patient with active epilepsy (treated or not) or in remission under treatment or without treatment for at least two years who died as a result of confirmed or probable SUDEP or NEAR SUDEP during the study period.

Controls : Patient with active epilepsy (treated or not) or in remission under treatment or without treatment for at least two years and matched by: age, epileptic syndrom and level of seizure controls

Exclusion criteria

Exclusion Criteria:

For cases and controls :patient not living in France, refusal of participation

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Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
408 participants (estimated)
Patient registry
No

Groups and cohorts

  • Cases

    Patient with epilepsy who died as a result of confirmed or probable SUDEP and NEAR SUDEP during the study period.

    Other: Interview with a psychologist and self-reported questionnaires

  • Controls

    Patient with epilepsy matched by: âge, etiology and type of epilepsy, level of seizure control

    Other: Interview with a psychologist and self-reported questionnaires

Interventions

  • OtherInterview with a psychologist and self-reported questionnaires

    The family members or patients who decide to participate in the study will be asked to complete an interview with a psychologist (semistructured interview, standard form, questionnaires) and self-reported questionnaires

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What researchers measure

Primary outcomes

  1. Risk factors for SUDEP

    * Lifestyle (night-time supervision ...), habits (alcohol consumption ...) * Personal cardiac history (arrhythmias, ECG abnormalities ...), respiratory, sleep apnoea, muscular or neurological disorders, mental retardation, associated psychiatric disorders... * Antiepileptic drugs

    Time frame: 1 day

Secondary outcomes

  1. Familial Risk factors for SUDEP

    Family history of epilepsy, Family history of sudden death, arrhythmias, sleep apnea

    Time frame: 1 day

  2. Needs and expectations of bereaved families on epilepsy related death information

    Time frame: 1 day

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Study locations

1 of 1 sites recruiting
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References and documents

Publications

  • Donner EJ, Waddell B, Osland K, Leach JP, Duncan S, Nashef L, Picot MC. After sudden unexpected death in epilepsy: Lessons learned and the road forward. Epilepsia. 2016 Jan;57 Suppl 1:46-53. doi: 10.1111/epi.13235. PubMed 26749016 ↗

Individual participant data

Plan to share: Yes — NC

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 8, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03074279
Lead sponsor
University Hospital, Montpellier
Collaborators
French Foundation for Epilepsy Research (FFRE), The French League Against Epilepsy (LFCE), University Hospital, Bordeaux, University Hospital, Lille, Hospices Civils de Lyon, University Hospital, Marseille, Central Hospital, Nancy, France, Paris AP-HP (La Pitié, St Anne, Necker, Robert Debré), Rennes University Hospital, University Hospital, Strasbourg, France, ToulouseUniversity Hospital
Responsible party
Sponsor
First posted
Mar 8, 2017
Start date
Jul 1, 2011
Primary completion
Dec 31, 2017 (estimated)
Completion
Jul 31, 2018 (estimated)
Last update
Mar 8, 2017

Study contacts

Marie-Christine Picot, MD, PhD
Contact
mc-picot@chu-montpellier.fr
467338978 ext. 33
Marie-Christine Picot, MD, PhD
study director · University Hospital, Montpellier

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2017. You cannot join it, but the record below documents what was studied.

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