Cerebral Micro Emboli Signal Detection in Endocarditis. A prospective follow-up study
- Conditions
- endocarditismicro embolie detectieontsteking van het weefsel van de hartkamer1001466210014523
- Registration Number
- NL-OMON54754
- Lead Sponsor
- HagaZiekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 100
1. Proven left-tailed infective native endocarditis or bioprosthetic valves
endocarditis
2. ultrasound test of the heart not older than 2 weeks
3. 18 years and older
4. mentally competent
5. written informed consent
1. right-tailed endocarditis
2. left-tailed endocarditis with already an emergency indication for
heartsurgery/valve replacement (<24h)
3. lack of a temporal window
4. severe claustrophobia or other MRI contraindications
5. Clinical manifistations of an old/recent CVA
6. mechanical valve
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary endpoint: development of a CVA during the hospitalization</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary neurological endpoints are:<br /><br>1. The severity of the CVA at origin and after 3 months (NIHSS score), the type<br /><br>of CVA (ischemic or hemorrhage)<br /><br>2. Occurrence of TIA's,<br /><br>3. Occurrence of meningitis,<br /><br>4. developing a cerebral abscess/cerebritis,<br /><br>5. mortality,<br /><br>6. functional outcome after 3 months<br /><br>7. SWI/DWI/Flair and T2 lesions on MRI brain (after 3 months or <24h prior to<br /><br>surgery) in compare with inclusion MRI.<br /><br>8. Occurrence of a heart surgery or valve surgery after inclusion.</p><br>