ID
11722
Beschrijving
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
Link
https://clinicaltrials.gov/ct2/show/NCT01084239
Trefwoorden
Versies (1)
- 28-07-15 28-07-15 -
Geüploaded op
28 juli 2015
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility ROMICAT-II Acute Coronary Syndrome NCT01084239
Eligibility Critera
- StudyEvent: ODM
Beschrijving
Exclusion Criteria
Beschrijving
New diagnostic ischemic ECG changes
Datatype
boolean
Alias
- UMLS CUI-1
- C0474715
Beschrijving
ST-segment elevation or depression > 1 mm
Datatype
boolean
Alias
- UMLS CUI-1
- C0520886
Beschrijving
T-wave inversion > 4 mm
Datatype
boolean
Alias
- UMLS CUI-1
- C0520888
Beschrijving
Documented or self-reported history of MI
Datatype
boolean
Alias
- UMLS CUI-1
- C1275835
Beschrijving
Documented or self-reported history of percutaneous coronary interventions [PCIs]
Datatype
boolean
Alias
- UMLS CUI-1
- C1320647
Beschrijving
Documented or self-reported history of coronary artery bypass graft [CABG]
Datatype
boolean
Alias
- UMLS CUI-1
- C1842251
Beschrijving
Documented or self-reported history of known significant coronary stenosis [>50%]
Datatype
boolean
Alias
- UMLS CUI-1
- C0242231
Beschrijving
Greater than 6 hours since presentation to ED.
Datatype
boolean
Alias
- UMLS CUI-1
- C1320532
Beschrijving
BMI >40 kg/m2
Datatype
boolean
Alias
- UMLS CUI-1
- C1305855
Beschrijving
Impaired renal function as defined by serum creatinine >1.5 mg/dL*
Datatype
boolean
Alias
- UMLS CUI-1
- C0035078
Beschrijving
Impaired renal function as defined by serum creatinine >1.5 mg/dL*
Datatype
boolean
Alias
- UMLS CUI-1
- C0201975
Beschrijving
Elevated troponin-T (> 0.09 ng/ml)
Datatype
boolean
Alias
- UMLS CUI-1
- C1141947
Beschrijving
Hemodynamically or clinically unstable condition (BP systolic < 80 mm Hg, atrial or ventricular arrhythmias, persistent chest pain despite adequate therapy)
Datatype
boolean
Alias
- UMLS CUI-1
- C0948268
Beschrijving
BP systolic < 80 mm Hg
Datatype
boolean
Alias
- UMLS CUI-1
- C0871470
Beschrijving
atrial or ventricular arrhythmias
Datatype
boolean
Alias
- UMLS CUI-1
- C0085612
- UMLS CUI-2
- C0085611
Beschrijving
persistent chest pain despite adequate therapy
Datatype
boolean
Alias
- UMLS CUI-1
- C0008031
Beschrijving
Known allergy to iodinated contrast agent
Datatype
boolean
Alias
- UMLS CUI-1
- C0570562
Beschrijving
Currently symptomatic asthma
Datatype
boolean
Alias
- UMLS CUI-1
- C0004096
Beschrijving
Documented or self-reported cocaine use within the past 48 hours (acute)
Datatype
boolean
Alias
- UMLS CUI-1
- C0239076
Beschrijving
On Metformin therapy and unable or unwilling to discontinue for 48 hours after the CT scan
Datatype
boolean
Alias
- UMLS CUI-1
- C0025598
Beschrijving
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
Datatype
boolean
Alias
- UMLS CUI-1
- C1278474
Beschrijving
Participant with no telephone or cell phone numbers or no address (preventing follow-up)
Datatype
boolean
Alias
- UMLS CUI-1
- C1515258
Beschrijving
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.
Datatype
boolean
Alias
- UMLS CUI-1
- C0549206
Beschrijving
Participant unwilling to provide a written informed consent.
Datatype
boolean
Alias
- UMLS CUI-1
- C0021430
Similar models
Eligibility Critera
- StudyEvent: ODM
C0085611 (UMLS CUI-2)