ID

28451

Beschreibung

The Effects of Tirofiban in Diabetic Patients Undergoing Elective Percutaneous Coronary Intervention; ODM derived from: https://clinicaltrials.gov/show/NCT00407771

Link

https://clinicaltrials.gov/show/NCT00407771

Stichworte

  1. 12.01.18 12.01.18 -
  2. 14.01.18 14.01.18 -
  3. 14.01.18 14.01.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

14. Januar 2018

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT00407771

Eligibility Coronary Artery Disease NCT00407771

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
diabetic patients with coronary artery disease undergoing elective percutaneous coronary intervention
Beschreibung

Patients Diabetic | Coronary Artery Disease | Percutaneous Coronary Intervention elective

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0241863
UMLS CUI [2]
C1956346
UMLS CUI [3,1]
C1532338
UMLS CUI [3,2]
C0439608
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
ongoing st-segment elevation myocardial infarction (mi)
Beschreibung

ST segment elevation myocardial infarction

Datentyp

boolean

Alias
UMLS CUI [1]
C1536220
administration of abciximab during the previous two weeks
Beschreibung

abciximab

Datentyp

boolean

Alias
UMLS CUI [1]
C0288672
serum creatinine more than 2.5 mg/dl (221 micro-mol/l)
Beschreibung

Creatinine measurement, serum

Datentyp

boolean

Alias
UMLS CUI [1]
C0201976
ongoing bleeding or bleeding diathesis
Beschreibung

Hemorrhage | Bleeding tendency

Datentyp

boolean

Alias
UMLS CUI [1]
C0019080
UMLS CUI [2]
C1458140
previous stroke in the last six months
Beschreibung

Cerebrovascular accident

Datentyp

boolean

Alias
UMLS CUI [1]
C0038454
major surgery within the previous six weeks
Beschreibung

Major surgery

Datentyp

boolean

Alias
UMLS CUI [1]
C0679637
platelet count <100.000 per cubic mm
Beschreibung

Platelet Count measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0032181
subjects who received low-molecular-weight heparin, tirofiban, or eptifibatide within the 10 hours prior to randomization
Beschreibung

Heparin, Low-Molecular-Weight | tirofiban | eptifibatide

Datentyp

boolean

Alias
UMLS CUI [1]
C0019139
UMLS CUI [2]
C0247025
UMLS CUI [3]
C0253563
subjects on oral anticoagulation medication (coumarin derivatives) within the last 7 days unless pt-inr <1.5 times the control
Beschreibung

Oral anticoagulants | Coumarins | Exception PT-INR Level

Datentyp

boolean

Alias
UMLS CUI [1]
C0354604
UMLS CUI [2]
C0010207
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C1821762
UMLS CUI [3,3]
C0441889

Ähnliche Modelle

Eligibility Coronary Artery Disease NCT00407771

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Patients Diabetic | Coronary Artery Disease | Percutaneous Coronary Intervention elective
Item
diabetic patients with coronary artery disease undergoing elective percutaneous coronary intervention
boolean
C0030705 (UMLS CUI [1,1])
C0241863 (UMLS CUI [1,2])
C1956346 (UMLS CUI [2])
C1532338 (UMLS CUI [3,1])
C0439608 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
ST segment elevation myocardial infarction
Item
ongoing st-segment elevation myocardial infarction (mi)
boolean
C1536220 (UMLS CUI [1])
abciximab
Item
administration of abciximab during the previous two weeks
boolean
C0288672 (UMLS CUI [1])
Creatinine measurement, serum
Item
serum creatinine more than 2.5 mg/dl (221 micro-mol/l)
boolean
C0201976 (UMLS CUI [1])
Hemorrhage | Bleeding tendency
Item
ongoing bleeding or bleeding diathesis
boolean
C0019080 (UMLS CUI [1])
C1458140 (UMLS CUI [2])
Cerebrovascular accident
Item
previous stroke in the last six months
boolean
C0038454 (UMLS CUI [1])
Major surgery
Item
major surgery within the previous six weeks
boolean
C0679637 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count <100.000 per cubic mm
boolean
C0032181 (UMLS CUI [1])
Heparin, Low-Molecular-Weight | tirofiban | eptifibatide
Item
subjects who received low-molecular-weight heparin, tirofiban, or eptifibatide within the 10 hours prior to randomization
boolean
C0019139 (UMLS CUI [1])
C0247025 (UMLS CUI [2])
C0253563 (UMLS CUI [3])
Oral anticoagulants | Coumarins | Exception PT-INR Level
Item
subjects on oral anticoagulation medication (coumarin derivatives) within the last 7 days unless pt-inr <1.5 times the control
boolean
C0354604 (UMLS CUI [1])
C0010207 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C1821762 (UMLS CUI [3,2])
C0441889 (UMLS CUI [3,3])

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