- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02854930
Near Death Experience (NDE) and Migraine
August 3, 2016 updated by: Assistance Publique Hopitaux De Marseille
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.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Marseille, France, 13354
- Assistance Publique Hôpitaux de Marseille Hôpital de la Timone
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
subject who experienced a near death experience (NDE).
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Quality of life
Time Frame: one day
|
one day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2017
Primary Completion (Anticipated)
January 1, 2018
Study Completion (Anticipated)
March 1, 2018
Study Registration Dates
First Submitted
August 1, 2016
First Submitted That Met QC Criteria
August 3, 2016
First Posted (Estimate)
August 4, 2016
Study Record Updates
Last Update Posted (Estimate)
August 4, 2016
Last Update Submitted That Met QC Criteria
August 3, 2016
Last Verified
August 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2014-47
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.