Internet Stroke Center Home Stroke Trials Registry
 
National Institute of Neurological Disorders & Stroke
American Stroke Association
Washington University School of Medicine
 
 Trials Directories
Ongoing Trials
Completed Trials
Acute Stroke Trials
Hemorrhage Trials
Prevention Trials
Recovery Trials
 Interventions
Drugs - By Name
Drugs - By Category
Procedures
Recovery Therapies
 Assessment Scales
Specific Stroke Scales
Stroke Scales Overview
 Stroke Trial Links
Government Sites
Independent Sites
 News & Updates
Update List
General Stroke News
About this Site
Submit Your Trial
Send Feedback

 Search for Trials

PubMed
We comply with the "Health on the Net" (HON) code of standards for trustworthy health information: verify here.



 
Stroke Interventions in Clinical Trials
Printable Version
SIFAP1
Stroke in Young Fabry Patients (SIFAP1): Frequency of Fabry Disease in Young Stroke Patients



Principal Investigator
Arndt Rolfs, Prof., MD

PI Address
Arndt Rolfs, Prof., MD
Department of
Neurology
University of
Rostock
POB 100 888, 18055
Rostock, Germany

Phone: +49-381-494- Ext. -9540
Email: arndt.rolfs@med.uni-rostock.de

Contact Address
1st Contact:
Dr. Gudrun Cimander, ClinSupport GmbH

Zweigstelle:
Julius-Echter-Weg 16
97762 Hammelburg
Tel +49/9723/787982
FAX +49/9732/787983
mobil +49/175/2956023
gudrun.cimander@clinsupport.de
2nd Contact:
Sabine Rösner
Deputy Head Dept. for Strategic Management
Neurobiology Laboratory
sifapTM-Project Coordinator
University of Rostock Dept. of Neurology

Gehlsheimerstrasse 20
18147 Rostock
Germany

Phone: +49-381-494- Ext. -4797

Sponsor



Study Size Actual:4244
Study Size Planned:5000
Centers Actual:45
Centers Planned:35
Max Time from onset:3 Months
Max Age:55
Min Age:18
ISRCTN#NCT00414583
Status:
Ongoing. Study began with a pilote phase in April 2007 and started in January 2008. Expected completion of the study is December 31, 2009.

Purpose:
To determine the frequency of Fabry disease in an unselected group of young stroke patients.

Location(s):
Austria, Belgium, Croatia, Finland, France, Georgian Republic, Germany, Italy, Malta, Poland, Portugal, Republic of Ireland, Spain, United Kingdom.

Year Started: 2008
Year Finished: 2009

Design:
Screening, cross-sectional, defined population, prospective study.

Inclusion Criteria
Patients with acute ischemic stroke or transient ischemic attack; MRI-scan evidence of associated corresponding brain infarction or hemorrhage, regardless of the duration of symptoms (also patients with no signs of stroke in the MRI can be included if a stroke-experienced neurologist has done the initial diagnosis as ischemic stroke, transient ischemic attack or hemorrhage); detailed MRI documentation at admission to entry to the study; diagnostic procedures for CVE according to the EUSI recommendations.

Exclusion Criteria
Acute ischemic stroke or transient ischemic attack longer than 3 months before enrolment into the study; diagnosis of the CVE within the last 3 months has been done by a non-neurologist if there is no MRI-scan evidence of associated brain infarction or hemorrhage; no detailed MR documentation at admission to entry to the study.

Primary Outcome:
Frequency of Fabry disease.

Source of Information:
ClinicalTrials.gov

Web Links and Publications:
Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study.
Lancet 2005 Nov 19;366(9499):1794-6

SIAFP-2
StrokeCenter.org

Stroke in young Fabry patients (SIFAP)

SIFAP1
ClinicalTrials.gov

This information last updated on: 10/7/2009

Reviewed on: 10/07/2009.

UID: 755

   

Internet Stroke Center at Washington University:
HOME | ABOUT | PRIVACY POLICY | CONTACT

Copyright © 1997-2009 - Internet Stroke Center. All rights reserved.                                           Last modified: Friday, November 20, 2009