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Prognostic Value of Circulating Endothelial Progenitor Cells in Aneurysmal Subarachnoid Hemorrhage

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)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01773200
Acronym
EVAPROPEC
Enrollment
92
Registered
2013-01-23
Start date
2013-03-31
Completion date
2018-03-31
Last updated
2016-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aneurysmal Subarachnoid Hemorrhage

Keywords

endothelial progenitor cells, aneurysmal subarachnoid hemorrhage, vasospasm, BNP

Brief summary

Aneurysmal subarachnoid hemorrhage is a common and serious disease associated to a high rate of mortality and morbidity. Severe definitive neurological impairment can concern up to 30% of patients in relation with elevated intracranial pressure, hemorrhage recurrence and symptomatic cerebral arterial vasospasm. This latter complication is defined as a reversible reduction of cerebral artery's diameter occurring between the 4th and the 14th day after bleeding. Physiopathology is not well understood, but could involve endothelium, trough endothelial progenitor cells (EPC). Circulating EPC are bone marrow-derived cells with capacity of vasculogenesis and angiogenesis. EPC have been recognized playing a beneficial role in cardiovascular disease and ischemic stroke. EPC have never been studied in aneurysmal subarachnoid hemorrhage. The primary objective of this study is to compare the number of circulating endothelial progenitor cells between patients with a good neurological outcome (defined as a glasgow outcome scale = 1 or 2) and patients with a poor neurological outcome (glasgow outcome scale = 3, 4 or 5). Briefly, the number of circulating EPC will be measured at admission, and at day 3, 6, 10, 14, 21 in each consecutive patient suffering aneurysmal subarachnoid hemorrhage and hospitalized in Teaching Hospital of Besançon (France). The neurological outcome will be measured one year after subarachnoid hemorrhage.

Interventions

None listed

Sponsors

Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
endothelial progenitor cells countday 3 after bleeding

Secondary

MeasureTime frame
Endothelial progenitor cells countday 0, 6, 10, 14, 21 after bleeding
Maximal amplitude of variation of EPC count3 weeks after bleeding
Plasmatic brain natriuretic peptideday 0, 3, 6, 10, 14, 21 after bleeding

Other

MeasureTime frameDescription
Glasgow Outcome ScaleOne year after bleeding
Vasospasm occurenceduring the 3 weeks after bleedingVasospasm will be defined as at less one segmental narrowing of a cerebral artery diagnosed on cerebral angiography (angio scanner, angio-MRI or 4 axes cerebral arteriography). Cerebral angiography will be done as necessary according to the occurence of the following situations * a clinical neurological deterioration unexplained by another cause * a mean arterial blood flow speed higher than 2 m/s assessed in cerebral arteries by transcranial doppler or a significant elevation of the mean arterial blood flow speed on two consecutive evaluations

Countries

France

Contacts

Primary ContactSébastien Pili-Floury, MD, PhD
spilifloury@orange.fr+33 3 81 66 85 79

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026