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Clinical Trial Summary

A monocentric, non-randomized, prospective study in which each patient is his/her own control.

The study investigates 2 methods of blood pressure measurement, within the first 24 hours after reperfusion, i) Continuous measurement of blood pressure with the Clearsight device (Edwards) and ii) intermittent blood pressure measurements with cuff.


Clinical Trial Description

Patients will be followed for 72 hours:

- inclusion after reperfusion: clinical evaluation with NIHSS (National Institute of Health Stroke Score) score, measurement of blood pressure.

- within 24 hours after reperfusion: blood pressure measurements

- at 24 hours: NIHSS score.

- Between 24 and 36 hours :cerebral scan (assessment of hemorrhagic transformations and cerebral infarction volumes).

- 72 hours after reperfusion: brain scanner in case of hyperdensity on the initial scanner ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03359434
Study type Interventional
Source Fondation Ophtalmologique Adolphe de Rothschild
Contact Laurence SALOMON, MD PhD
Phone 01.48.03.64.31
Email lsalomon@for.paris
Status Not yet recruiting
Phase N/A
Start date September 2018
Completion date March 2021

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