NCT02572297

Brief Summary

Sudden unexpected death in epilepsy (SUDEP) is the main concern of professionals and patient associations involved in epilepsy. These represent a priority for the Ligue Française Contre l'Epilepsie (LFCE). The SUDEP affect primarily young adults, between 18 and 40 years, suffering from epilepsy uncontrolled by medication. In this population of close to 100,000 people in France, the incidence of SUDEP is estimated at 0.5%, or nearly 500 deaths per year. It is clear that the majority of these deaths occur in the immediate consequences of a crisis.. Investigators suppose that a causal link exists between the occurrence of a SUDEP and a per / post-critic decline of SpO2 below 80 % (75 % of cases, 20 % of controls).The constitution of a cohort of 1500 patients clinically well described and a national database will allow other ambitious projects in a speciality where French centres benefit from a unique knowledge, recognized by their foreign colleagues, but underexploited to date. The LFCE (Ligue Française Contre l'Epilepsie) is developing structuring actions to facilitate such exploratory studies for the next two years. The high death rate which characterizes the drug-resistant partial epilepsies and, in particular, Sudden Unexpected Deaths in Epilepsy (SUDEP) represents the main axis of research for the Ligue Française Contre l'Epilepsie (LFCE) as well as for associations of epileptic patients and the European representatives of the international league against epilepsy ( ILAE). Today, SUDEP occurrences cannot be anticipated. Patients can't be warned against SUDEP. Although the SUDEP physiopathology remains uncertain, many elements plead for the essential role of a per-and post-critic apnea (central or obstructive). Investigators observe that about 20 % of the patients admitted in a EEG-video monitoring - EEG unit for recording their crisis are going to present experience an per / post-critic severe apnea, severe per / post-critic enough to have induce a SpO2 \< 80 % decrease. However, today, no study has estimated the link relation between the arisen occurrence of such apneas and the later risk of SUDEP.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,072

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2010

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 18, 2010

Completed
4.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2015

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 23, 2015

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

September 4, 2015

Completed
1 month until next milestone

First Posted

Study publicly available on registry

October 8, 2015

Completed
Last Updated

December 19, 2025

Status Verified

December 1, 2025

Enrollment Period

4.7 years

First QC Date

September 4, 2015

Last Update Submit

December 13, 2025

Conditions

Keywords

epilepsySUDEPSpO2

Outcome Measures

Primary Outcomes (1)

  • Number of patients with SpO2 < 80% decreases during the EEG-video monitoring

    To establish a relation between the occurence of SpO2 \< 80% decreases during a EEG-video monitoring and the later risk of SUDEP.

    6 and a half months

Secondary Outcomes (2)

  • Frequence of other known potential risk factors (composite measure : presence rate of each risk factor in SUDEP measured as percentage)

    6 and a half months

  • Allelic frequency of genes involved in epileptogenesis (measured as percentage)

    6 and a half months

Study Arms (1)

video-EEG

Patients suffering from drug-resistant partial epilepsy for whom a video-EEG monitoring of their seizures was scheduled as part of pre-surgical assessment

Other: video-EEG

Interventions

Registration of seizures during video-EEG

video-EEG

Eligibility Criteria

Age15 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients suffering from drud-resistant partial epilepsy whom a video-EEG monitoring of their seizures was scheduled as part of a pre-surgical assessment

You may qualify if:

  • patients suffering from drud-resistant partial epilepsy ;
  • Patients who are at least 15 years ;
  • Patients for whom a video-EEG monitoring of their seizures was scheduled as part of a pre-surgical assessment ;
  • Patients having a registration number in the RNIP (Répertoire National d'Identification des Personnes Physiques) or a Social Security number
  • Patients who have given their written consent ;
  • Patients with a social security

You may not qualify if:

  • Patients under 15 years
  • Patients without drug-resistant partial epilepsy
  • Patients without a registration number in the RNIP (Répertoire National d'Identification des Personnes Physiques) or a Social Security number)
  • Patient without a consent signed

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Service de Neurologie Fonctionnelle et d'Epileptologie, Hôpital Pierre Wertheimer, Hospices Civils de Lyon

Bron, 69677, France

Location

MeSH Terms

Conditions

EpilepsySudden Unexpected Death in Epilepsy

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System DiseasesDeath, SuddenDeathPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Philippe RYVLIN, MD

    Sercie de neurologie fonctionnelle et d'epileptologie, Hôpital Neurologique Pierre Wertheimer

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
10 Years
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 4, 2015

First Posted

October 8, 2015

Study Start

May 18, 2010

Primary Completion

February 1, 2015

Study Completion

August 23, 2015

Last Updated

December 19, 2025

Record last verified: 2025-12

Locations