ID
12469
Description
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
Lien
https://clinicaltrials.gov/ct2/show/NCT01035047
Mots-clés
Versions (2)
- 28/07/2015 28/07/2015 -
- 21/11/2015 21/11/2015 -
Téléchargé le
21 novembre 2015
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility Chest Pain Diagnostic Acute Coronary Syndrome NCT01035047
Eligibility Criteria
- StudyEvent: ODM
Description
Exclusion criteria
Description
Elevated cardiac biomarkers
Type de données
boolean
Alias
- UMLS CUI-1
- C0741921
Description
New ST-segment elevation on any electrocardiogram (>/= 1 mV)
Type de données
boolean
Alias
- UMLS CUI-1
- C0520886
Description
New ST-segment depression on any electrocardiogram (>/= 2 mV)
Type de données
boolean
Alias
- UMLS CUI-1
- C0520887
Description
Known inducible cardiac ischemia without subsequent revascularization
Type de données
boolean
Alias
- UMLS CUI-1
- C0151744
Description
Unable to lie flat
Type de données
boolean
Alias
- UMLS CUI [1]
- C1717946
Description
Symptomatic hypotension at the time of enrollment (systolic < 90 mm Hg)
Type de données
boolean
Alias
- UMLS CUI-1
- C0020649
Description
Contra-indications to MRI (examples: Pacemaker, defibrillator, cerebral aneurysm clips, metallic ocular foreign body, implanted devices, severe claustrophobia)
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0024485
- UMLS CUI [1,2]
- C0522473
Description
Terminal diagnosis with life expectancy less than 3 months
Type de données
boolean
Alias
- UMLS CUI-1
- C0679247
Description
Currently Pregnant
Type de données
boolean
Alias
- UMLS CUI-1
- C0549206
Description
Creatinine clearance < 45 ml/min at the time of enrollment or clinical concern for acute kidney injury
Type de données
boolean
Alias
- UMLS CUI-1
- C0373595
Description
Chronic liver disease with a creatinine clearance of <60 ml/min at the time of enrollment
Type de données
boolean
Alias
- UMLS CUI-1
- C0085605
Description
Hepato-renal syndrome
Type de données
boolean
Alias
- UMLS CUI-1
- C0019212
Description
History of liver transplant
Type de données
boolean
Alias
- UMLS CUI-1
- C0023911
Description
History of heart transplant
Type de données
boolean
Alias
- UMLS CUI-1
- C0018823
Description
History of kidney transplant
Type de données
boolean
Alias
- UMLS CUI-1
- C0022671
Description
Confirmed angioplasty
Type de données
boolean
Alias
- UMLS CUI-1
- C0190211
Description
Confirmed stent placement within the last 6 months
Type de données
boolean
Alias
- UMLS CUI-1
- C3272316
Description
Confirmed coronary artery bypass grafting (CABG) within the last 6 months
Type de données
boolean
Alias
- UMLS CUI-1
- C0010055
Similar models
Eligibility Criteria
- StudyEvent: ODM
C0522473 (UMLS CUI [1,2])