Prospective Study Evaluating the Interest of Long-term Cardiac Recording in Cerebral Infarction

NACompletedINTERVENTIONAL
Enrollment

108

Participants

Timeline

Start Date

November 17, 2014

Primary Completion Date

July 31, 2018

Study Completion Date

April 24, 2019

Conditions
Neuropathology
Interventions
DEVICE

Uses of SpiderFlash monitor

"Investigators will use the SpiderFlash®, Holter monitor (technology Secure Data) to have a storage capacity enabling a registration up to 30 days with sufficient autonomy.~The data collected :~* Demographic data: age, sex, vascular risk factors, antithrombotic therapy at the entrance, history of Transient Ischemic Accident (TIA) or Cerebral infarct (CI)~* Data on the CI:~* Monitoring Results scope ICU Neurovascular.~* Presence palpitations~* Treatment influencing the rate (beta-blockers or antiarrhythmic)~* Data on cardiac monitoring:~A questionnaire evaluating the safety of SpiderFlash® will be given to the patient and the results of Holter will be communicated at the end of the recording to the blinded rhythm specialist"

Trial Locations (1)

75014

Groupe Hospitalier Paris Saint Joseph, Paris

All Listed Sponsors
lead

Fondation Hôpital Saint-Joseph

OTHER

NCT02778321 - Prospective Study Evaluating the Interest of Long-term Cardiac Recording in Cerebral Infarction | Biotech Hunter | Biotech Hunter