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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02854930
Other study ID # 2014-47
Secondary ID
Status Not yet recruiting
Phase N/A
First received August 1, 2016
Last updated August 3, 2016
Start date January 2017
Est. completion date March 2018

Study information

Verified date August 2016
Source Assistance Publique Hopitaux De Marseille
Contact Anne Donnet
Phone 0491382747
Email drci@ap-hm.fr
Is FDA regulated No
Health authority France: Comité consultatif sur le traitement de l'information en matière de recherche dans le domaine de la santé
Study type Observational

Clinical Trial Summary

Migraine is a common disabling primary headache disorder. Epidemiological studies have documented its high prevalence and high socio-economic and personal impacts. Migraine affects more than 20% of the French population. However, the physiopathology of migraine is always partially known. Cortical spreading depression (CSD) is the widely accepted as the electrophysiologic substrate of migraine aura. CSD is a slowly propagating wave of transient neuronal and glial depolarization. The near death experience (NDE) is a rare, but well known phenomenon. NDE are profound psychic experiences commonly occuring in life-threatening conditions. Among the neurological hypotheses, epilepsy, temporal lobe disorders , REM-sleep intrusion have been discussed. However, the role of DCE has never been discussed. The goals of this study are : to see if there is an epidemiological link between NDE and migraine/ to specify if NDE was followed by a migrainous headache.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date March 2018
Est. primary completion date January 2018
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Subject who experienced an NDE defined by the occurrence, when the subject is in a state of clinical death or a particular state of consciousness of a following event: body output experience, disembodiment, for a tunnel and / or light;

- Topic recorded in the EMI database (Dr. Postel, National Center for Education, Research and Information on the conscience;

- Topic agreeing to participate in the study.

Exclusion Criteria:

- Patient mental condition or disorder or psychiatric history or any other factor limiting the ability to participate in an informed manner and compliant to the study;

- Other than obtained Participation Agreement.

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
questioning


Locations

Country Name City State
France Assistance Publique Hôpitaux de Marseille Hôpital de la Timone Marseille

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of life one day No
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