Last update : 06/28/2014 | Version : 1 | ID : 60057
General | |
Identification | |
Detailed name | Treatment for Subarachnoid Haemorrhage from Ruptured Aneurysm: National Cohort Study |
Sign or acronym | SAH |
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation | CNIL : 10/01/2008 |
General Aspects | |
Medical area |
Neurology |
Others (details) | Subarachnoid haemorrhage |
Keywords | Neurological moribidity, death, hospitalisation |
Scientific investigator(s) (Contact) | |
Name of the director | Guillemin |
Surname | Francis |
Phone | + 33 (0)3 83 85 21 63 |
francis.guillemin@chu-nancy.fr | |
Unit | CENTRE D'EPIDEMIOLOGIE CLINIQUE CIC-EC INSERM CIE 6, NANCY |
Organization | CHU de |
Name of the director | AUDIBERT |
Unit | CENTRE D'EPIDEMIOLOGIE CLINIQUE CIC-EC INSERM CIE 6, NANCY |
Name of the director | PUYBASSET |
Collaborations | |
Funding | |
Funding status |
Mixed |
Details | CHU DE NANCY, ANARFL |
Governance of the database | |
Sponsor(s) or organisation(s) responsible | CHU de Nancy |
Organisation status |
Public |
Additional contact | |
Main features | |
Type of database | |
Type of database |
Study databases |
Study databases (details) |
Cohort study |
Database recruitment is carried out by an intermediary |
A selection of health institutions and services |
Database recruitment is carried out as part of an interventional study |
No |
Additional information regarding sample selection. | Inclusion method: Prospective Inclusion cut-off date: 01/10/2009 |
Database objective | |
Main objective | Objective general: to identify prognostic factors of mortality and neurological morbidity in patients suffering a subarachnoid haemorrhage (SAH) from an aneurysmal rupture who arrive alive at hospital. - to describe characteristics, medical treatment and neurologic outcome for these subjects; - to define poor prognostic factors. |
Inclusion criteria | Adult patients hospitalised for a subarachnoid haemorrhage from an aneurysmal rupture. |
Population type | |
Age |
Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) Elderly (65 to 79 years) Great age (80 years and more) |
Population covered |
Sick population |
Gender |
Male Woman |
Geography area |
National |
Detail of the geography area | Multicentric cohort (30 centres): France (including overseas territories) |
Data collection | |
Dates | |
Date of first collection (YYYY or MM/YYYY) | 10/2007 |
Date of last collection (YYYY or MM/YYYY) | 10/2010 |
Size of the database | |
Size of the database (number of individuals) |
[1000-10 000[ individuals |
Details of the number of individuals | 2100 |
Data | |
Database activity |
Data collection completed |
Type of data collected |
Clinical data |
Clinical data (detail) |
Direct physical measures Medical registration |
Presence of a biobank |
No |
Health parameters studied |
Health event/morbidity Health event/mortality |
Procedures | |
Data collection method | Cinical examinations: manual input |
Participant monitoring |
Yes |
Details on monitoring of participants | Follow-up duration: 12 months |
Links to administrative sources |
No |
Promotion and access | |
Promotion | |
Access | |
Terms of data access (charter for data provision, format of data, availability delay) | Data may not be used by academic teams Data may not be used by industrial teams |
Access to aggregated data |
Access on specific project only |
Access to individual data |
No access |
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