DRKS00016852
Completed
Not Applicable
Berlin Longterm Observation of Vascular Events - Pilot study - BeLOVE - Pilot study
ConditionsI21I61I63E11N17I67.6H34.1H47.0G45.0G45.1G45.2G45.3G45.9I11.0I13.0I13.2I13.9I42I50.0I50.13I50.14I50.19I50.9Acute myocardial infarctionIntracerebral haemorrhageCerebral infarctionType 2 diabetes mellitusAcute renal failureNonpyogenic thrombosis of intracranial venous systemCentral retinal artery occlusionDisorders of optic nerve, not elsewhere classifiedVertebro-basilar artery syndromeCarotid artery syndrome (hemispheric)Multiple and bilateral precerebral artery syndromesAmaurosis fugaxTransient cerebral ischaemic attack, unspecifiedHypertensive heart disease with (congestive) heart failureHypertensive heart and renal disease with (congestive) heart failureHypertensive heart and renal disease with both (congestive) heart failure and renal failureHypertensive heart and renal disease, unspecifiedCardiomyopathyCongestive heart failureHeart failure, unspecified
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- I21
- Sponsor
- Charité Universitätsmedizin Berlin
- Enrollment
- 2248
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •provision of signed and dated informed consent form
- •2\)declared willingness to take part in study procedures and to be contacted again for further
- •follow\-up examinations
- •3\)persons of any sex and gender, aged 18 years or above at the time of acute event or study
- •4\)general health status is acceptable for participation in a study
- •5\)clinical diagnosis of one or more of the following diseases:
- •A) acute heart failure (trigger event), defined by:
- •i) dyspnoe NYHA IIIb or IV and NTproBNP \= 300 pg/nl OR
- •MRproANP \= 120 pmol/l, AND
- •ii)evidence of pitting peripheral edema or radiological or clinical signs of
Exclusion Criteria
- •1\) lack of capacity to give informed consent
- •2\) pregnancy or lactation
- •3\) life expectancy \< 6 months due to non\-cardio\-/cerebrovascular diseases or conditions
- •4\) organ transplanted
- •5\) Lack of health insurance
Outcomes
Primary Outcomes
Not specified
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Berlin Longterm Observation of Vascular EventsI21I61I63N17H34.1G45.0G45.1G45.2G45.3G45.9I11.0I13.0I13.2I13.9I42I50I50.13I50.14I50.19I50.9I10.0I10.1I10.9E78.0E78.1E78.2E78.5I70.2I70.8I25.1N18.3N18.4N18.5H35.0H36.0G63.2Acute myocardial infarctionIntracerebral haemorrhageCerebral infarctionAcute renal failureCentral retinal artery occlusionVertebro-basilar artery syndromeCarotid artery syndrome (hemispheric)Multiple and bilateral precerebral artery syndromesAmaurosis fugaxTransient cerebral ischaemic attack, unspecifiedHypertensive heart disease with (congestive) heart failureHypertensive heart and renal disease with (congestive) heart failureHypertensive heart and renal disease with both (congestive) heart failure and renal failureHypertensive heart and renal disease, unspecifiedCardiomyopathyHeart failureHeart failure, unspecifiedPure hypercholesterolaemiaPure hyperglyceridaemiaMixed hyperlipidaemiaHyperlipidaemia, unspecifiedAtherosclerosis of arteries of extremitiesAtherosclerosis of other arteriesAtherosclerotic heart diseaseChronic kidney disease, stage 3Chronic kidney disease, stage 4Chronic kidney disease, stage 5Background retinopathy and retinal vascular changesDiabetic retinopathyDiabetic polyneuropathyDRKS00023323Charité Campus Charité Mitte8,000
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