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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01917955
Other study ID # CaMriSS_CSB
Secondary ID EA4/073/10
Status Completed
Phase N/A
First received August 7, 2012
Last updated November 7, 2016
Start date January 2012
Est. completion date November 2014

Study information

Verified date November 2016
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority Germany: Ministry of Health
Study type Observational

Clinical Trial Summary

The purpose of this prospective single-center trial is to compare the safety and diagnostic value of contrast medium-enhanced cardiac magnetic resonance imaging and transesophageal echocardiography in patients with acute ischemic stroke.


Description:

Primary safety objective: Contrast medium-enhanced cardiac magnetic resonance imaging is safe in patients with acute ischemic stroke. Primary outcome: The diagnostic value of contrast medium-enhanced cardiac magnetic resonance imaging is comparable to transesophageal echocardiography in patients with acute ischemic stroke.


Recruitment information / eligibility

Status Completed
Enrollment 103
Est. completion date November 2014
Est. primary completion date November 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with acute ischemic stroke detected by brain magnetic resonance imaging.

Exclusion Criteria:

- Known atrial fibrillation or cardiac source of embolism

- Severe aphasia

- Acute infection or chronic inflammation

- Severe arteriosclerosis or stenosis of brain-supplying arteries

- Contraindications for magnetic resonance imaging or transesophageal echocardiography.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Charité, Universitätsmedizin Berlin, Campus Benjamin Franklin Berlin
Germany Elisabeth Hospital Essen

Sponsors (3)

Lead Sponsor Collaborator
Charite University, Berlin, Germany Cardiology and Angiology, Elisabeth Hospital, Essen, Germany, Center for Stroke Research Berlin

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sensitivity and specificity of contrast medium-enhanced cardiac magnetic resonance imaging to detect echocardiography-proven cardiac sources of embolism in patients with acute ischemic stroke. < 1 week after ischemic stroke No
Secondary Rate of unrecognised myocardial infarction detected by late gadolinium-enhanced cardiac MRI in patients with acute ischemic stroke. < 1 week after ischemic stroke No
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