ID
11722
Description
The growing availability of cardiac computed tomography (CT)* in emergency departments (EDs) across the U.S. expands the opportunities for its clinical application, but also heightens the need to define its appropriate use in the evaluation of patients with acute chest pain. To address this need, we performed a randomized diagnostic trial (RDT) to determine whether integrating cardiac CT, along with the information it provides on coronary artery disease (CAD) and left ventricular (LV) function, can improve the efficiency of the management of these patients (i.e. shorten length of hospital stay, increase direct discharge rates from the ED, decreasing healthcare costs and improving cost effectiveness while being safe). https://clinicaltrials.gov/ct2/show/NCT01084239
Lien
https://clinicaltrials.gov/ct2/show/NCT01084239
Mots-clés
Versions (1)
- 28/07/2015 28/07/2015 -
Téléchargé le
28 juillet 2015
DOI
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Licence
Creative Commons BY 4.0
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Eligibility ROMICAT-II Acute Coronary Syndrome NCT01084239
Eligibility Critera
- StudyEvent: ODM
Description
Exclusion Criteria
Description
New diagnostic ischemic ECG changes
Type de données
boolean
Alias
- UMLS CUI-1
- C0474715
Description
ST-segment elevation or depression > 1 mm
Type de données
boolean
Alias
- UMLS CUI-1
- C0520886
Description
T-wave inversion > 4 mm
Type de données
boolean
Alias
- UMLS CUI-1
- C0520888
Description
Documented or self-reported history of MI
Type de données
boolean
Alias
- UMLS CUI-1
- C1275835
Description
Documented or self-reported history of percutaneous coronary interventions [PCIs]
Type de données
boolean
Alias
- UMLS CUI-1
- C1320647
Description
Documented or self-reported history of coronary artery bypass graft [CABG]
Type de données
boolean
Alias
- UMLS CUI-1
- C1842251
Description
Documented or self-reported history of known significant coronary stenosis [>50%]
Type de données
boolean
Alias
- UMLS CUI-1
- C0242231
Description
Greater than 6 hours since presentation to ED.
Type de données
boolean
Alias
- UMLS CUI-1
- C1320532
Description
BMI >40 kg/m2
Type de données
boolean
Alias
- UMLS CUI-1
- C1305855
Description
Impaired renal function as defined by serum creatinine >1.5 mg/dL*
Type de données
boolean
Alias
- UMLS CUI-1
- C0035078
Description
Impaired renal function as defined by serum creatinine >1.5 mg/dL*
Type de données
boolean
Alias
- UMLS CUI-1
- C0201975
Description
Elevated troponin-T (> 0.09 ng/ml)
Type de données
boolean
Alias
- UMLS CUI-1
- C1141947
Description
Hemodynamically or clinically unstable condition (BP systolic < 80 mm Hg, atrial or ventricular arrhythmias, persistent chest pain despite adequate therapy)
Type de données
boolean
Alias
- UMLS CUI-1
- C0948268
Description
BP systolic < 80 mm Hg
Type de données
boolean
Alias
- UMLS CUI-1
- C0871470
Description
atrial or ventricular arrhythmias
Type de données
boolean
Alias
- UMLS CUI-1
- C0085612
- UMLS CUI-2
- C0085611
Description
persistent chest pain despite adequate therapy
Type de données
boolean
Alias
- UMLS CUI-1
- C0008031
Description
Known allergy to iodinated contrast agent
Type de données
boolean
Alias
- UMLS CUI-1
- C0570562
Description
Currently symptomatic asthma
Type de données
boolean
Alias
- UMLS CUI-1
- C0004096
Description
Documented or self-reported cocaine use within the past 48 hours (acute)
Type de données
boolean
Alias
- UMLS CUI-1
- C0239076
Description
On Metformin therapy and unable or unwilling to discontinue for 48 hours after the CT scan
Type de données
boolean
Alias
- UMLS CUI-1
- C0025598
Description
Contraindication to beta blockers (taking daily antiasthmatic medication): This exclusion only applies to patients with a heart rate >65 bpm at sites using a non-dual source CT scanner
Type de données
boolean
Alias
- UMLS CUI-1
- C1278474
Description
Participant with no telephone or cell phone numbers or no address (preventing follow-up)
Type de données
boolean
Alias
- UMLS CUI-1
- C1515258
Description
Participant with positive pregnancy test. Women of childbearing potential, defined as <2 years of menopause in the absence of hysterectomy or tube ligation, must have a pregnancy test performed within 24 hours before the CT scan.
Type de données
boolean
Alias
- UMLS CUI-1
- C0549206
Description
Participant unwilling to provide a written informed consent.
Type de données
boolean
Alias
- UMLS CUI-1
- C0021430
Similar models
Eligibility Critera
- StudyEvent: ODM
C0085611 (UMLS CUI-2)