ID
12469
Beschreibung
Clinical decision units (CDUs) improve resource utilization and are a recommended care option by the American College of Cardiology / American Heart Association, but are underutilized in non-low risk chest pain patients due to weaknesses of traditional cardiac testing. Cardiac magnetic resonance imaging (CMR) is sensitive and specific for ischemia, can simultaneously assess cardiac function and myocardial perfusion, and could revolutionize the diagnostic process for intermediate risk patients with chest pain. The primary objective of this trial is to measure the efficiency and safety of a combined CDU-CMR care pathway compared to inpatient care among patients with non-low risk acute chest pain. https://clinicaltrials.gov/ct2/show/NCT01035047
Link
https://clinicaltrials.gov/ct2/show/NCT01035047
Stichworte
Versionen (2)
- 28.07.15 28.07.15 -
- 21.11.15 21.11.15 -
Hochgeladen am
21. November 2015
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Chest Pain Diagnostic Acute Coronary Syndrome NCT01035047
Eligibility Criteria
- StudyEvent: ODM
Beschreibung
Exclusion criteria
Beschreibung
Elevated cardiac biomarkers
Datentyp
boolean
Alias
- UMLS CUI-1
- C0741921
Beschreibung
New ST-segment elevation on any electrocardiogram (>/= 1 mV)
Datentyp
boolean
Alias
- UMLS CUI-1
- C0520886
Beschreibung
New ST-segment depression on any electrocardiogram (>/= 2 mV)
Datentyp
boolean
Alias
- UMLS CUI-1
- C0520887
Beschreibung
Known inducible cardiac ischemia without subsequent revascularization
Datentyp
boolean
Alias
- UMLS CUI-1
- C0151744
Beschreibung
Unable to lie flat
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1717946
Beschreibung
Symptomatic hypotension at the time of enrollment (systolic < 90 mm Hg)
Datentyp
boolean
Alias
- UMLS CUI-1
- C0020649
Beschreibung
Contra-indications to MRI (examples: Pacemaker, defibrillator, cerebral aneurysm clips, metallic ocular foreign body, implanted devices, severe claustrophobia)
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0024485
- UMLS CUI [1,2]
- C0522473
Beschreibung
Terminal diagnosis with life expectancy less than 3 months
Datentyp
boolean
Alias
- UMLS CUI-1
- C0679247
Beschreibung
Currently Pregnant
Datentyp
boolean
Alias
- UMLS CUI-1
- C0549206
Beschreibung
Creatinine clearance < 45 ml/min at the time of enrollment or clinical concern for acute kidney injury
Datentyp
boolean
Alias
- UMLS CUI-1
- C0373595
Beschreibung
Chronic liver disease with a creatinine clearance of <60 ml/min at the time of enrollment
Datentyp
boolean
Alias
- UMLS CUI-1
- C0085605
Beschreibung
Hepato-renal syndrome
Datentyp
boolean
Alias
- UMLS CUI-1
- C0019212
Beschreibung
History of liver transplant
Datentyp
boolean
Alias
- UMLS CUI-1
- C0023911
Beschreibung
History of heart transplant
Datentyp
boolean
Alias
- UMLS CUI-1
- C0018823
Beschreibung
History of kidney transplant
Datentyp
boolean
Alias
- UMLS CUI-1
- C0022671
Beschreibung
Confirmed angioplasty
Datentyp
boolean
Alias
- UMLS CUI-1
- C0190211
Beschreibung
Confirmed stent placement within the last 6 months
Datentyp
boolean
Alias
- UMLS CUI-1
- C3272316
Beschreibung
Confirmed coronary artery bypass grafting (CABG) within the last 6 months
Datentyp
boolean
Alias
- UMLS CUI-1
- C0010055
Ähnliche Modelle
Eligibility Criteria
- StudyEvent: ODM
C0522473 (UMLS CUI [1,2])