Gender | Percutaneous Coronary Intervention elective Scheduled | Parameters cardiac Absent | Unfractionated heparin therapy Absent
Item
males or females scheduled for non-urgent elective pci (who do not have certain cardiac parameters) and have not been treated with uhf prior to pci.
boolean
C0079399 (UMLS CUI [1])
C1532338 (UMLS CUI [2,1])
C0439608 (UMLS CUI [2,2])
C0205539 (UMLS CUI [2,3])
C0449381 (UMLS CUI [3,1])
C0018787 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C4076594 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Informed Consent | Protocol Compliance
Item
subject able to give informed consent and comply with the protocol.
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Urine pregnancy test negative | Female Sterilization | Menopausal
Item
negative urine pregnancy test or documented surgical sterilization or menopausal.
boolean
C0430057 (UMLS CUI [1])
C0015787 (UMLS CUI [2])
C0025320 (UMLS CUI [3])
Body Weight
Item
subject weight >120 kg.
boolean
C0005910 (UMLS CUI [1])
Acute Coronary Syndrome | Cardiac markers Elevated | ST segment depression At rest
Item
recent acute coronary syndrome with elevated cardiac markers or st segment depression at rest.
boolean
C0948089 (UMLS CUI [1])
C1271630 (UMLS CUI [2,1])
C3163633 (UMLS CUI [2,2])
C0520887 (UMLS CUI [3,1])
C0443144 (UMLS CUI [3,2])
Instability Clinical
Item
evidence of clinical instability
boolean
C1444783 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
Angiography High risk
Item
angiographic high-risk.
boolean
C0002978 (UMLS CUI [1,1])
C0332167 (UMLS CUI [1,2])
Medical contraindication Anticoagulation Therapy | High risk of bleeding
Item
a contraindication to anticoagulation or increased risk of bleeding.
boolean
C1301624 (UMLS CUI [1,1])
C0003281 (UMLS CUI [1,2])
C4039184 (UMLS CUI [2])
Illicit drug use | Investigational New Drugs
Item
use of prohibited medications or investigational drugs prior to the study.
boolean
C0281875 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
Laboratory test result abnormal
Item
clinically significant abnormal laboratory findings.
boolean
C0438215 (UMLS CUI [1])
Band Tissue Femoral Size | Use Planned
Item
planned use of femoral sheath greater than a certain size.
boolean
C0175723 (UMLS CUI [1,1])
C0040300 (UMLS CUI [1,2])
C0015811 (UMLS CUI [1,3])
C0456389 (UMLS CUI [1,4])
C1524063 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Hypersensitivity Investigational New Drugs | Intolerance to Investigational New Drugs
Item
known allergy or intolerance to drugs mandated by the study.
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Medical Devices Use of | Angioplasty Balloon Excluded | Coronary stent Excluded
Item
use of devices other than angioplasty balloons and coronary stents.
boolean
C0025080 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
C0002996 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
C0687568 (UMLS CUI [3,1])
C2828389 (UMLS CUI [3,2])
Drug abuse | Illicit drug use
Item
a history of licit drug abuse or illicit drug use or current evidence of such abuse.
boolean
C0013146 (UMLS CUI [1])
C0281875 (UMLS CUI [2])
Factor Study Subject Participation Status At risk Increased
Item
any other factor that the investigator feels would put the subject at increased risk if participating in the protocol.
boolean
C1521761 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,3])
C0205217 (UMLS CUI [1,4])
Breast Feeding
Item
lactation.
boolean
C0006147 (UMLS CUI [1])
Study Subject Participation Status
Item
currently enrolled in this or another clinical trial (with some exceptions).
boolean
C2348568 (UMLS CUI [1])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
participation in an investigational drug or device trial in the past 30 days.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])