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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 11 April 2016
Main ID:  NCT01773200
Date of registration: 18/01/2013
Prospective Registration: Yes
Primary sponsor: Centre Hospitalier Universitaire de Besancon
Public title: Prognostic Value of Circulating Endothelial Progenitor Cells in Aneurysmal Subarachnoid Hemorrhage EVAPROPEC
Scientific title: Prognostic Value of Circulating Endothelial Progenitor Cells in Aneurysmal Subarachnoid Hemorrhage (Evaluation de l'intérêt Pronostic Des progéniteurs endothéliaux Circulants Dans l'hémorragie Sous-arachnoïdienne Par Rupture d'anévrysme cérébral)
Date of first enrolment: March 2013
Target sample size: 92
Recruitment status: Recruiting
URL:  https://clinicaltrials.gov/show/NCT01773200
Study type:  Observational
Study design:  Observational Model: Cohort, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
France
Contacts
Name:     Sébastien Pili-Floury, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  CHRU de Besançon
Name:     Sébastien Pili-Floury, MD, PhD
Address: 
Telephone: +33 3 81 66 85 79
Email: spilifloury@orange.fr
Affiliation: 
Key inclusion & exclusion criteria

Inclusion Criteria:

- recent(< 24 h) aneurysmal subarachnoid hemorrhage

- written informed consent obtained from the patient or from close relatives

Exclusion Criteria:

- refusal to participate

- Non-aneurysmal subarachnoid hemorrhage

- aneurysmal subarachnoid hemorrhage with estimated date of bleeding > 24 h

- Chronic heart failure

- Chronic medication able to modify the plasmatic level of BNP

- Pregnancy



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Aneurysmal Subarachnoid Hemorrhage
Intervention(s)
Primary Outcome(s)
endothelial progenitor cells count [Time Frame: day 3 after bleeding]
Secondary Outcome(s)
Endothelial progenitor cells count [Time Frame: day 0, 6, 10, 14, 21 after bleeding]
Plasmatic brain natriuretic peptide [Time Frame: day 0, 3, 6, 10, 14, 21 after bleeding]
Maximal amplitude of variation of EPC count [Time Frame: 3 weeks after bleeding]
Secondary ID(s)
P/2012/153
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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