BRUSH Sign: Radiolographic Marker of Cerebral Infarctus Prognosis

Sponsor
Groupe Hospitalier Paris Saint Joseph (Other)
Overall Status
Completed
CT.gov ID
NCT03467269
Collaborator
(none)
250
1
4.1
60.4

Study Details

Study Description

Brief Summary

Today the treatment of ischemic stroke in acute phase is based on medicinal or endovascular revascularization. Cerebral MRI sequences help the diagnostic. This procedure uses deoxyhemoglobin as an endogenous tracer. This is also a scorer of cerebral ischemia and the increase lets visualized transcerebral veins in the suffering zone giving a brush aspect. Several studies show the interest of this sign and conclude that deoxyhemoglobin presence is a predictive factor of cerebral ischemia. The aim of the study is to evaluate this brush-sign and correlate it with the prognosis retrospectively.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Brush sign

Study Design

Study Type:
Observational
Actual Enrollment :
250 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
BRUSH Sign: Radiolographic Marker of Cerebral Infarctus Prognosis
Actual Study Start Date :
Feb 24, 2017
Actual Primary Completion Date :
Apr 1, 2017
Actual Study Completion Date :
Jun 30, 2017

Outcome Measures

Primary Outcome Measures

  1. autonomy level [Month 3]

    measurement of autonomy level by mRS

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • age>18 years old

  • hospitalized for cerebral infarction

  • MCA territory

  • MRI within 24hours

  • Sequence of magnetic susceptibility (SWAN)

Exclusion Criteria:
  • Incomplete cerebral infarct

  • MRI not possible

Contacts and Locations

Locations

Site City State Country Postal Code
1 Groupe Hospitalier Paris Saint Joseph Paris Ile-de-France France 75014

Sponsors and Collaborators

  • Groupe Hospitalier Paris Saint Joseph

Investigators

  • Principal Investigator: ZUBER Mathieu, Professor, GHPSJ

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Groupe Hospitalier Paris Saint Joseph
ClinicalTrials.gov Identifier:
NCT03467269
Other Study ID Numbers:
  • BRUSH SIGN
First Posted:
Mar 15, 2018
Last Update Posted:
Mar 15, 2018
Last Verified:
Mar 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 15, 2018